Canonical Allele Identifier: CA366742033
Gene: PMS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1008261
ClinVar RCV Id: RCV001305565
dbSNP Id: rs587781827

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5987341A>C , CM000669.2:g.5987341A>C GRCh38
NC_000007.13:g.6026972A>C , CM000669.1:g.6026972A>C GRCh37
NC_000007.12:g.5993498A>C NCBI36
NG_008466.1:g.26766T>G , LRG_161:g.26766T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000699814.2:c.*820T>G ENSP00000514615.2:n.*820T>G
ENST00000699840.2:c.1421T>G ENSP00000514638.2:p.Val474Gly
ENST00000699930.2:c.1316T>G ENSP00000514695.2:p.Val439Gly
ENST00000406569.8:c.1424T>G ENSP00000514464.1:p.Val475Gly
ENST00000644110.2:c.*1018T>G ENSP00000496392.2:n.*1018T>G
ENST00000699752.1:c.1268T>G ENSP00000514561.1:p.Val423Gly
ENST00000699753.1:c.*845T>G ENSP00000514562.1:n.*845T>G
ENST00000699754.1:c.1226T>G ENSP00000514563.1:p.Val409Gly
ENST00000699755.1:c.*823T>G ENSP00000514564.1:n.*823T>G
ENST00000699756.1:c.*1011T>G ENSP00000514565.1:n.*1011T>G
ENST00000699757.1:c.*681T>G ENSP00000514566.1:n.*681T>G
ENST00000699758.1:c.*681T>G ENSP00000514567.1:n.*681T>G
ENST00000699759.1:n.2278T>G
ENST00000699760.1:c.1106T>G ENSP00000514568.1:p.Val369Gly
ENST00000699761.1:c.1019T>G ENSP00000514569.1:p.Val340Gly
ENST00000699762.1:c.851T>G ENSP00000514570.1:p.Val284Gly
ENST00000699763.1:c.*514T>G ENSP00000514571.1:n.*514T>G
ENST00000699764.1:c.1424T>G ENSP00000514572.1:p.Val475Gly
ENST00000699765.1:c.*520T>G ENSP00000514573.1:n.*520T>G
ENST00000699766.1:c.1424T>G ENSP00000514574.1:p.Val475Gly
ENST00000699767.1:c.1424T>G ENSP00000514575.1:p.Val475Gly
ENST00000699768.1:c.1424T>G ENSP00000514576.1:p.Val475Gly
ENST00000699811.1:c.1019T>G ENSP00000514614.1:p.Val340Gly
ENST00000699813.1:n.1537T>G
ENST00000699814.1:c.1047T>G
ENST00000699815.1:c.*955T>G ENSP00000514616.1:n.*955T>G
ENST00000699816.1:c.*314T>G ENSP00000514617.1:n.*314T>G
ENST00000699817.1:c.*1018T>G ENSP00000514618.1:n.*1018T>G
ENST00000699818.1:c.1019T>G ENSP00000514619.1:p.Val340Gly
ENST00000699819.1:c.*581T>G ENSP00000514620.1:n.*581T>G
ENST00000699820.1:c.1144+2459T>G ENSP00000514621.1:n.1144+2459T>G
ENST00000699821.1:c.1019T>G ENSP00000514622.1:p.Val340Gly
ENST00000699822.1:c.*876T>G ENSP00000514623.1:n.*876T>G
ENST00000699823.1:c.1019T>G ENSP00000514624.1:p.Val340Gly
ENST00000699824.1:c.*927T>G ENSP00000514625.1:n.*927T>G
ENST00000699825.1:c.863T>G ENSP00000514626.1:p.Val288Gly
ENST00000699826.1:c.*823T>G ENSP00000514627.1:n.*823T>G
ENST00000699827.1:c.1256T>G ENSP00000514628.1:p.Val419Gly
ENST00000699828.1:c.*514T>G ENSP00000514629.1:n.*514T>G
ENST00000699833.1:n.3196T>G
ENST00000699837.1:c.1019T>G ENSP00000514635.1:p.Val340Gly
ENST00000699838.1:c.*1324T>G ENSP00000514636.1:n.*1324T>G
ENST00000699839.1:c.1610T>G ENSP00000514637.1:p.Val537Gly
ENST00000699916.1:c.*681T>G ENSP00000514684.1:n.*681T>G
ENST00000699917.1:c.*873T>G ENSP00000514685.1:n.*873T>G
ENST00000699918.1:c.*925T>G ENSP00000514686.1:n.*925T>G
ENST00000699919.1:c.*1011T>G ENSP00000514687.1:n.*1011T>G
ENST00000699920.1:c.*1060T>G ENSP00000514688.1:n.*1060T>G
ENST00000699928.1:c.989-4350T>G ENSP00000514693.1:n.989-4350T>G
ENST00000699929.1:c.*725T>G ENSP00000514694.1:n.*725T>G
ENST00000699930.1:c.1316T>G ENSP00000514695.1:p.Val439Gly
ENST00000699931.1:n.2852T>G
ENST00000699951.1:c.*520T>G ENSP00000514706.1:n.*520T>G
ENST00000699952.1:c.803+9985T>G ENSP00000514707.1:n.803+9985T>G
ENST00000699953.1:c.*531T>G ENSP00000514708.1:n.*531T>G
ENST00000699954.1:c.*725T>G ENSP00000514709.1:n.*725T>G
ENST00000265849.12:c.1424T>G MANE Select ENSP00000265849.7:p.Val475Gly
ENST00000642292.1:c.1019T>G ENSP00000495524.1:p.Val340Gly
ENST00000642456.1:c.1019T>G ENSP00000493814.1:p.Val340Gly
ENST00000643595.1:c.*823T>G ENSP00000494497.1:n.*823T>G
ENST00000644110.1:c.1106T>G ENSP00000496392.1:p.Val369Gly
ENST00000265849.11:c.1424T>G ENSP00000265849.7:p.Val475Gly
ENST00000382321.5:c.804-4350T>G ENSP00000371758.4:n.804-4350T>G
ENST00000406569.7:n.1424T>G
ENST00000441476.6:c.1106T>G ENSP00000392843.2:p.Val369Gly
ENST00000469652.1:n.63-4436T>G
NM_000535.5:c.1424T>G , LRG_161t1:c.1424T>G NP_000526.1:p.Val475Gly
NR_003085.2:n.1506T>G
XM_006715742.2:c.1418T>G XP_006715805.1:p.Val473Gly
XM_006715744.2:c.491T>G XP_006715807.1:p.Val164Gly
XM_011515427.1:c.1469T>G XP_011513729.1:p.Val490Gly
XM_011515428.1:c.1313T>G XP_011513730.1:p.Val438Gly
XM_011515429.1:c.1106T>G XP_011513731.1:p.Val369Gly
XM_011515430.1:c.1106T>G XP_011513732.1:p.Val369Gly
NM_000535.6:c.1424T>G NP_000526.2:p.Val475Gly
NM_001322003.1:c.1019T>G NP_001308932.1:p.Val340Gly
NM_001322004.1:c.1019T>G NP_001308933.1:p.Val340Gly
NM_001322005.1:c.1019T>G NP_001308934.1:p.Val340Gly
NM_001322006.1:c.1268T>G NP_001308935.1:p.Val423Gly
NM_001322007.1:c.1106T>G NP_001308936.1:p.Val369Gly
NM_001322008.1:c.1106T>G NP_001308937.1:p.Val369Gly
NM_001322009.1:c.1019T>G NP_001308938.1:p.Val340Gly
NM_001322010.1:c.863T>G NP_001308939.1:p.Val288Gly
NM_001322011.1:c.491T>G NP_001308940.1:p.Val164Gly
NM_001322012.1:c.491T>G NP_001308941.1:p.Val164Gly
NM_001322013.1:c.851T>G NP_001308942.1:p.Val284Gly
NM_001322014.1:c.1424T>G NP_001308943.1:p.Val475Gly
NM_001322015.1:c.1115T>G NP_001308944.1:p.Val372Gly
NR_136154.1:n.1511T>G
XM_006715744.4:c.491T>G XP_006715807.1:p.Val164Gly
XM_017012342.2:c.491T>G XP_016867831.1:p.Val164Gly
XM_024446800.1:c.863T>G XP_024302568.1:p.Val288Gly
NM_000535.7:c.1424T>G MANE Select NP_000526.2:p.Val475Gly
NM_001322003.2:c.1019T>G NP_001308932.1:p.Val340Gly
NM_001322004.2:c.1019T>G NP_001308933.1:p.Val340Gly
NM_001322005.2:c.1019T>G NP_001308934.1:p.Val340Gly
NM_001322006.2:c.1268T>G NP_001308935.1:p.Val423Gly
NM_001322008.2:c.1106T>G NP_001308937.1:p.Val369Gly
NM_001322009.2:c.1019T>G NP_001308938.1:p.Val340Gly
NM_001322010.2:c.863T>G NP_001308939.1:p.Val288Gly
NM_001322011.2:c.491T>G NP_001308940.1:p.Val164Gly
NM_001322012.2:c.491T>G NP_001308941.1:p.Val164Gly
NM_001322013.2:c.851T>G NP_001308942.1:p.Val284Gly
NM_001322014.2:c.1424T>G NP_001308943.1:p.Val475Gly
NM_001322015.2:c.1115T>G NP_001308944.1:p.Val372Gly
NM_001322007.2:c.1106T>G NP_001308936.1:p.Val369Gly