Canonical Allele Identifier: CA366741947
Gene: PMS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1772833
ClinVar RCV Id: RCV002394489
dbSNP Id: rs2128730424

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5987317T>C , CM000669.2:g.5987317T>C GRCh38
NC_000007.13:g.6026948T>C , CM000669.1:g.6026948T>C GRCh37
NC_000007.12:g.5993474T>C NCBI36
NG_008466.1:g.26790A>G , LRG_161:g.26790A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000699814.2:c.*844A>G ENSP00000514615.2:n.*844A>G
ENST00000699840.2:c.1445A>G ENSP00000514638.2:p.Asp482Gly
ENST00000699930.2:c.1340A>G ENSP00000514695.2:p.Asp447Gly
ENST00000406569.8:c.1448A>G ENSP00000514464.1:p.Asp483Gly
ENST00000644110.2:c.*1042A>G ENSP00000496392.2:n.*1042A>G
ENST00000699752.1:c.1292A>G ENSP00000514561.1:p.Asp431Gly
ENST00000699753.1:c.*869A>G ENSP00000514562.1:n.*869A>G
ENST00000699754.1:c.1250A>G ENSP00000514563.1:p.Asp417Gly
ENST00000699755.1:c.*847A>G ENSP00000514564.1:n.*847A>G
ENST00000699756.1:c.*1035A>G ENSP00000514565.1:n.*1035A>G
ENST00000699757.1:c.*705A>G ENSP00000514566.1:n.*705A>G
ENST00000699758.1:c.*705A>G ENSP00000514567.1:n.*705A>G
ENST00000699759.1:n.2302A>G
ENST00000699760.1:c.1130A>G ENSP00000514568.1:p.Asp377Gly
ENST00000699761.1:c.1043A>G ENSP00000514569.1:p.Asp348Gly
ENST00000699762.1:c.875A>G ENSP00000514570.1:p.Asp292Gly
ENST00000699763.1:c.*538A>G ENSP00000514571.1:n.*538A>G
ENST00000699764.1:c.1448A>G ENSP00000514572.1:p.Asp483Gly
ENST00000699765.1:c.*544A>G ENSP00000514573.1:n.*544A>G
ENST00000699766.1:c.1448A>G ENSP00000514574.1:p.Asp483Gly
ENST00000699767.1:c.1448A>G ENSP00000514575.1:p.Asp483Gly
ENST00000699768.1:c.1448A>G ENSP00000514576.1:p.Asp483Gly
ENST00000699811.1:c.1043A>G ENSP00000514614.1:p.Asp348Gly
ENST00000699813.1:n.1561A>G
ENST00000699814.1:c.1071A>G
ENST00000699815.1:c.*979A>G ENSP00000514616.1:n.*979A>G
ENST00000699816.1:c.*338A>G ENSP00000514617.1:n.*338A>G
ENST00000699817.1:c.*1042A>G ENSP00000514618.1:n.*1042A>G
ENST00000699818.1:c.1043A>G ENSP00000514619.1:p.Asp348Gly
ENST00000699819.1:c.*605A>G ENSP00000514620.1:n.*605A>G
ENST00000699820.1:c.1144+2483A>G ENSP00000514621.1:n.1144+2483A>G
ENST00000699821.1:c.1043A>G ENSP00000514622.1:p.Asp348Gly
ENST00000699822.1:c.*900A>G ENSP00000514623.1:n.*900A>G
ENST00000699823.1:c.1043A>G ENSP00000514624.1:p.Asp348Gly
ENST00000699824.1:c.*951A>G ENSP00000514625.1:n.*951A>G
ENST00000699825.1:c.887A>G ENSP00000514626.1:p.Asp296Gly
ENST00000699826.1:c.*847A>G ENSP00000514627.1:n.*847A>G
ENST00000699827.1:c.1280A>G ENSP00000514628.1:p.Asp427Gly
ENST00000699828.1:c.*538A>G ENSP00000514629.1:n.*538A>G
ENST00000699833.1:n.3220A>G
ENST00000699837.1:c.1043A>G ENSP00000514635.1:p.Asp348Gly
ENST00000699838.1:c.*1348A>G ENSP00000514636.1:n.*1348A>G
ENST00000699839.1:c.1634A>G ENSP00000514637.1:p.Asp545Gly
ENST00000699916.1:c.*705A>G ENSP00000514684.1:n.*705A>G
ENST00000699917.1:c.*897A>G ENSP00000514685.1:n.*897A>G
ENST00000699918.1:c.*949A>G ENSP00000514686.1:n.*949A>G
ENST00000699919.1:c.*1035A>G ENSP00000514687.1:n.*1035A>G
ENST00000699920.1:c.*1084A>G ENSP00000514688.1:n.*1084A>G
ENST00000699928.1:c.989-4326A>G ENSP00000514693.1:n.989-4326A>G
ENST00000699929.1:c.*749A>G ENSP00000514694.1:n.*749A>G
ENST00000699930.1:c.1340A>G ENSP00000514695.1:p.Asp447Gly
ENST00000699931.1:n.2876A>G
ENST00000699951.1:c.*544A>G ENSP00000514706.1:n.*544A>G
ENST00000699952.1:c.803+10009A>G ENSP00000514707.1:n.803+10009A>G
ENST00000699953.1:c.*555A>G ENSP00000514708.1:n.*555A>G
ENST00000699954.1:c.*749A>G ENSP00000514709.1:n.*749A>G
ENST00000265849.12:c.1448A>G MANE Select ENSP00000265849.7:p.Asp483Gly
ENST00000642292.1:c.1043A>G ENSP00000495524.1:p.Asp348Gly
ENST00000642456.1:c.1043A>G ENSP00000493814.1:p.Asp348Gly
ENST00000643595.1:c.*847A>G ENSP00000494497.1:n.*847A>G
ENST00000644110.1:c.1130A>G ENSP00000496392.1:p.Asp377Gly
ENST00000265849.11:c.1448A>G ENSP00000265849.7:p.Asp483Gly
ENST00000382321.5:c.804-4326A>G ENSP00000371758.4:n.804-4326A>G
ENST00000406569.7:n.1448A>G
ENST00000441476.6:c.1130A>G ENSP00000392843.2:p.Asp377Gly
ENST00000469652.1:n.63-4412A>G
NM_000535.5:c.1448A>G , LRG_161t1:c.1448A>G NP_000526.1:p.Asp483Gly
NR_003085.2:n.1530A>G
XM_006715742.2:c.1442A>G XP_006715805.1:p.Asp481Gly
XM_006715744.2:c.515A>G XP_006715807.1:p.Asp172Gly
XM_011515427.1:c.1493A>G XP_011513729.1:p.Asp498Gly
XM_011515428.1:c.1337A>G XP_011513730.1:p.Asp446Gly
XM_011515429.1:c.1130A>G XP_011513731.1:p.Asp377Gly
XM_011515430.1:c.1130A>G XP_011513732.1:p.Asp377Gly
NM_000535.6:c.1448A>G NP_000526.2:p.Asp483Gly
NM_001322003.1:c.1043A>G NP_001308932.1:p.Asp348Gly
NM_001322004.1:c.1043A>G NP_001308933.1:p.Asp348Gly
NM_001322005.1:c.1043A>G NP_001308934.1:p.Asp348Gly
NM_001322006.1:c.1292A>G NP_001308935.1:p.Asp431Gly
NM_001322007.1:c.1130A>G NP_001308936.1:p.Asp377Gly
NM_001322008.1:c.1130A>G NP_001308937.1:p.Asp377Gly
NM_001322009.1:c.1043A>G NP_001308938.1:p.Asp348Gly
NM_001322010.1:c.887A>G NP_001308939.1:p.Asp296Gly
NM_001322011.1:c.515A>G NP_001308940.1:p.Asp172Gly
NM_001322012.1:c.515A>G NP_001308941.1:p.Asp172Gly
NM_001322013.1:c.875A>G NP_001308942.1:p.Asp292Gly
NM_001322014.1:c.1448A>G NP_001308943.1:p.Asp483Gly
NM_001322015.1:c.1139A>G NP_001308944.1:p.Asp380Gly
NR_136154.1:n.1535A>G
XM_006715744.4:c.515A>G XP_006715807.1:p.Asp172Gly
XM_017012342.2:c.515A>G XP_016867831.1:p.Asp172Gly
XM_024446800.1:c.887A>G XP_024302568.1:p.Asp296Gly
NM_000535.7:c.1448A>G MANE Select NP_000526.2:p.Asp483Gly
NM_001322003.2:c.1043A>G NP_001308932.1:p.Asp348Gly
NM_001322004.2:c.1043A>G NP_001308933.1:p.Asp348Gly
NM_001322005.2:c.1043A>G NP_001308934.1:p.Asp348Gly
NM_001322006.2:c.1292A>G NP_001308935.1:p.Asp431Gly
NM_001322008.2:c.1130A>G NP_001308937.1:p.Asp377Gly
NM_001322009.2:c.1043A>G NP_001308938.1:p.Asp348Gly
NM_001322010.2:c.887A>G NP_001308939.1:p.Asp296Gly
NM_001322011.2:c.515A>G NP_001308940.1:p.Asp172Gly
NM_001322012.2:c.515A>G NP_001308941.1:p.Asp172Gly
NM_001322013.2:c.875A>G NP_001308942.1:p.Asp292Gly
NM_001322014.2:c.1448A>G NP_001308943.1:p.Asp483Gly
NM_001322015.2:c.1139A>G NP_001308944.1:p.Asp380Gly
NM_001322007.2:c.1130A>G NP_001308936.1:p.Asp377Gly