Canonical Allele Identifier: CA366734674
Gene: PMS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525654
ClinVar RCV Id: RCV000629806
dbSNP Id: rs1554292688
gnomAD v4: 7-5973400-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5973400C>A , CM000669.2:g.5973400C>A GRCh38
NC_000007.13:g.6013031C>A , CM000669.1:g.6013031C>A GRCh37
NC_000007.12:g.5979557C>A NCBI36
NG_008466.1:g.40707G>T , LRG_161:g.40707G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699814.2:c.*1984G>T ENSP00000514615.2:n.*1984G>T
ENST00000699840.2:c.2585G>T ENSP00000514638.2:p.Ter862Leu
ENST00000699930.2:c.2480G>T ENSP00000514695.2:p.Ter827Leu
ENST00000406569.8:c.1948G>T ENSP00000514464.1:n.1948G>T
ENST00000644110.2:c.*2182G>T ENSP00000496392.2:n.*2182G>T
ENST00000699752.1:c.2432G>T ENSP00000514561.1:p.Ter811Leu
ENST00000699753.1:c.*2009G>T ENSP00000514562.1:n.*2009G>T
ENST00000699754.1:c.2390G>T ENSP00000514563.1:p.Ter797Leu
ENST00000699755.1:c.*1987G>T ENSP00000514564.1:n.*1987G>T
ENST00000699756.1:c.*2175G>T ENSP00000514565.1:n.*2175G>T
ENST00000699757.1:c.*1845G>T ENSP00000514566.1:n.*1845G>T
ENST00000699758.1:c.*1845G>T ENSP00000514567.1:n.*1845G>T
ENST00000699759.1:n.3442G>T
ENST00000699760.1:c.2270G>T ENSP00000514568.1:p.Ter757Leu
ENST00000699761.1:c.2183G>T ENSP00000514569.1:p.Ter728Leu
ENST00000699762.1:c.2015G>T ENSP00000514570.1:p.Ter672Leu
ENST00000699763.1:c.*1678G>T ENSP00000514571.1:n.*1678G>T
ENST00000699764.1:c.*906G>T ENSP00000514572.1:n.*906G>T
ENST00000699765.1:c.*1583G>T ENSP00000514573.1:n.*1583G>T
ENST00000699766.1:c.2621G>T ENSP00000514574.1:p.Ter874Leu
ENST00000699767.1:c.*229G>T ENSP00000514575.1:n.*229G>T
ENST00000699768.1:c.2444G>T ENSP00000514576.1:p.Ter815Leu
ENST00000699811.1:c.2183G>T ENSP00000514614.1:p.Ter728Leu
ENST00000699813.1:n.2701G>T
ENST00000699814.1:c.2211G>T
ENST00000699815.1:c.*2119G>T ENSP00000514616.1:n.*2119G>T
ENST00000699816.1:c.*1478G>T ENSP00000514617.1:n.*1478G>T
ENST00000699817.1:c.*2182G>T ENSP00000514618.1:n.*2182G>T
ENST00000699818.1:c.2183G>T ENSP00000514619.1:p.Ter728Leu
ENST00000699819.1:c.*1745G>T ENSP00000514620.1:n.*1745G>T
ENST00000699820.1:c.*526G>T ENSP00000514621.1:n.*526G>T
ENST00000699821.1:c.2216G>T ENSP00000514622.1:p.Ter739Leu
ENST00000699822.1:c.*2040G>T ENSP00000514623.1:n.*2040G>T
ENST00000699823.1:c.2183G>T ENSP00000514624.1:p.Ter728Leu
ENST00000699824.1:c.*2091G>T ENSP00000514625.1:n.*2091G>T
ENST00000699825.1:c.2027G>T ENSP00000514626.1:p.Ter676Leu
ENST00000699826.1:c.*1987G>T ENSP00000514627.1:n.*1987G>T
ENST00000699827.1:c.2420G>T ENSP00000514628.1:p.Ter807Leu
ENST00000699828.1:c.*1678G>T ENSP00000514629.1:n.*1678G>T
ENST00000699833.1:n.4360G>T
ENST00000699837.1:c.2183G>T ENSP00000514635.1:p.Ter728Leu
ENST00000699838.1:c.*2488G>T ENSP00000514636.1:n.*2488G>T
ENST00000699839.1:c.2774G>T ENSP00000514637.1:p.Ter925Leu
ENST00000699916.1:c.*1845G>T ENSP00000514684.1:n.*1845G>T
ENST00000699917.1:c.*2037G>T ENSP00000514685.1:n.*2037G>T
ENST00000699918.1:c.*2089G>T ENSP00000514686.1:n.*2089G>T
ENST00000699919.1:c.*2175G>T ENSP00000514687.1:n.*2175G>T
ENST00000699920.1:c.*2224G>T ENSP00000514688.1:n.*2224G>T
ENST00000699928.1:c.*526G>T ENSP00000514693.1:n.*526G>T
ENST00000699951.1:c.*1641G>T ENSP00000514706.1:n.*1641G>T
ENST00000699952.1:c.*142G>T ENSP00000514707.1:n.*142G>T
ENST00000265849.12:c.2588G>T MANE Select ENSP00000265849.7:p.Ter863Leu
ENST00000642292.1:c.2183G>T ENSP00000495524.1:p.Ter728Leu
ENST00000642456.1:c.2183G>T ENSP00000493814.1:p.Ter728Leu
ENST00000643595.1:c.*1987G>T ENSP00000494497.1:n.*1987G>T
ENST00000644110.1:c.2270G>T ENSP00000496392.1:p.Ter757Leu
ENST00000265849.11:c.2588G>T ENSP00000265849.7:p.Ter863Leu
ENST00000382321.5:c.1385G>T ENSP00000371758.4:p.Ter462Leu
ENST00000441476.6:c.2270G>T ENSP00000392843.2:p.Ter757Leu
NM_000535.5:c.2588G>T , LRG_161t1:c.2588G>T NP_000526.1:p.Ter863Leu
NR_003085.2:n.2670G>T
XM_006715742.2:c.2582G>T XP_006715805.1:p.Ter861Leu
XM_006715744.2:c.1655G>T XP_006715807.1:p.Ter552Leu
XM_011515427.1:c.2633G>T XP_011513729.1:p.Ter878Leu
XM_011515428.1:c.2477G>T XP_011513730.1:p.Ter826Leu
XM_011515429.1:c.2270G>T XP_011513731.1:p.Ter757Leu
XM_011515430.1:c.2270G>T XP_011513732.1:p.Ter757Leu
NM_000535.6:c.2588G>T NP_000526.2:p.Ter863Leu
NM_001322003.1:c.2183G>T NP_001308932.1:p.Ter728Leu
NM_001322004.1:c.2183G>T NP_001308933.1:p.Ter728Leu
NM_001322005.1:c.2183G>T NP_001308934.1:p.Ter728Leu
NM_001322006.1:c.2432G>T NP_001308935.1:p.Ter811Leu
NM_001322007.1:c.2270G>T NP_001308936.1:p.Ter757Leu
NM_001322008.1:c.2270G>T NP_001308937.1:p.Ter757Leu
NM_001322009.1:c.2216G>T NP_001308938.1:p.Ter739Leu
NM_001322010.1:c.2027G>T NP_001308939.1:p.Ter676Leu
NM_001322011.1:c.1655G>T NP_001308940.1:p.Ter552Leu
NM_001322012.1:c.1655G>T NP_001308941.1:p.Ter552Leu
NM_001322013.1:c.2015G>T NP_001308942.1:p.Ter672Leu
NM_001322014.1:c.2621G>T NP_001308943.1:p.Ter874Leu
NM_001322015.1:c.2279G>T NP_001308944.1:p.Ter760Leu
NR_136154.1:n.2632G>T
XM_006715744.4:c.1655G>T XP_006715807.1:p.Ter552Leu
XM_017012342.2:c.1655G>T XP_016867831.1:p.Ter552Leu
XM_024446800.1:c.2027G>T XP_024302568.1:p.Ter676Leu
NM_000535.7:c.2588G>T MANE Select NP_000526.2:p.Ter863Leu
NM_001322003.2:c.2183G>T NP_001308932.1:p.Ter728Leu
NM_001322004.2:c.2183G>T NP_001308933.1:p.Ter728Leu
NM_001322005.2:c.2183G>T NP_001308934.1:p.Ter728Leu
NM_001322006.2:c.2432G>T NP_001308935.1:p.Ter811Leu
NM_001322008.2:c.2270G>T NP_001308937.1:p.Ter757Leu
NM_001322009.2:c.2216G>T NP_001308938.1:p.Ter739Leu
NM_001322010.2:c.2027G>T NP_001308939.1:p.Ter676Leu
NM_001322011.2:c.1655G>T NP_001308940.1:p.Ter552Leu
NM_001322012.2:c.1655G>T NP_001308941.1:p.Ter552Leu
NM_001322013.2:c.2015G>T NP_001308942.1:p.Ter672Leu
NM_001322014.2:c.2621G>T NP_001308943.1:p.Ter874Leu
NM_001322015.2:c.2279G>T NP_001308944.1:p.Ter760Leu
NM_001322007.2:c.2270G>T NP_001308936.1:p.Ter757Leu