Canonical Allele Identifier: CA1685230551
Gene: PMS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5987439T= , CM000669.2:g.5987439T= GRCh38
NC_000007.13:g.6027070T= , CM000669.1:g.6027070T= GRCh37
NC_000007.12:g.5993596T= NCBI36
NG_008466.1:g.26668A= , LRG_161:g.26668A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000699814.2:c.*722A= ENSP00000514615.2:n.*722A=
ENST00000699840.2:c.1323A= ENSP00000514638.2:p.Pro441=
ENST00000699930.2:c.1218A= ENSP00000514695.2:p.Pro406=
ENST00000406569.8:c.1326A= ENSP00000514464.1:p.Pro442=
ENST00000644110.2:c.*920A= ENSP00000496392.2:n.*920A=
ENST00000699752.1:c.1170A= ENSP00000514561.1:p.Pro390=
ENST00000699753.1:c.*747A= ENSP00000514562.1:n.*747A=
ENST00000699754.1:c.1128A= ENSP00000514563.1:p.Pro376=
ENST00000699755.1:c.*725A= ENSP00000514564.1:n.*725A=
ENST00000699756.1:c.*913A= ENSP00000514565.1:n.*913A=
ENST00000699757.1:c.*583A= ENSP00000514566.1:n.*583A=
ENST00000699758.1:c.*583A= ENSP00000514567.1:n.*583A=
ENST00000699759.1:n.2180A=
ENST00000699760.1:c.1008A= ENSP00000514568.1:p.Pro336=
ENST00000699761.1:c.921A= ENSP00000514569.1:p.Pro307=
ENST00000699762.1:c.753A= ENSP00000514570.1:p.Pro251=
ENST00000699763.1:c.*416A= ENSP00000514571.1:n.*416A=
ENST00000699764.1:c.1326A= ENSP00000514572.1:p.Pro442=
ENST00000699765.1:c.*422A= ENSP00000514573.1:n.*422A=
ENST00000699766.1:c.1326A= ENSP00000514574.1:p.Pro442=
ENST00000699767.1:c.1326A= ENSP00000514575.1:p.Pro442=
ENST00000699768.1:c.1326A= ENSP00000514576.1:p.Pro442=
ENST00000699811.1:c.921A= ENSP00000514614.1:p.Pro307=
ENST00000699813.1:n.1439A=
ENST00000699814.1:c.949A=
ENST00000699815.1:c.*857A= ENSP00000514616.1:n.*857A=
ENST00000699816.1:c.*216A= ENSP00000514617.1:n.*216A=
ENST00000699817.1:c.*920A= ENSP00000514618.1:n.*920A=
ENST00000699818.1:c.921A= ENSP00000514619.1:p.Pro307=
ENST00000699819.1:c.*483A= ENSP00000514620.1:n.*483A=
ENST00000699820.1:c.1144+2361A= ENSP00000514621.1:n.1144+2361A=
ENST00000699821.1:c.921A= ENSP00000514622.1:p.Pro307=
ENST00000699822.1:c.*778A= ENSP00000514623.1:n.*778A=
ENST00000699823.1:c.921A= ENSP00000514624.1:p.Pro307=
ENST00000699824.1:c.*829A= ENSP00000514625.1:n.*829A=
ENST00000699825.1:c.765A= ENSP00000514626.1:p.Pro255=
ENST00000699826.1:c.*725A= ENSP00000514627.1:n.*725A=
ENST00000699827.1:c.1158A= ENSP00000514628.1:p.Pro386=
ENST00000699828.1:c.*416A= ENSP00000514629.1:n.*416A=
ENST00000699833.1:n.3098A=
ENST00000699837.1:c.921A= ENSP00000514635.1:p.Pro307=
ENST00000699838.1:c.*1226A= ENSP00000514636.1:n.*1226A=
ENST00000699839.1:c.1512A= ENSP00000514637.1:p.Pro504=
ENST00000699916.1:c.*583A= ENSP00000514684.1:n.*583A=
ENST00000699917.1:c.*775A= ENSP00000514685.1:n.*775A=
ENST00000699918.1:c.*827A= ENSP00000514686.1:n.*827A=
ENST00000699919.1:c.*913A= ENSP00000514687.1:n.*913A=
ENST00000699920.1:c.*962A= ENSP00000514688.1:n.*962A=
ENST00000699928.1:c.989-4448A= ENSP00000514693.1:n.989-4448A=
ENST00000699929.1:c.*627A= ENSP00000514694.1:n.*627A=
ENST00000699930.1:c.1218A= ENSP00000514695.1:p.Pro406=
ENST00000699931.1:n.2754A=
ENST00000699951.1:c.*422A= ENSP00000514706.1:n.*422A=
ENST00000699952.1:c.803+9887A= ENSP00000514707.1:n.803+9887A=
ENST00000699953.1:c.*433A= ENSP00000514708.1:n.*433A=
ENST00000699954.1:c.*627A= ENSP00000514709.1:n.*627A=
ENST00000265849.12:c.1326A= MANE Select ENSP00000265849.7:p.Pro442=
ENST00000642292.1:c.921A= ENSP00000495524.1:p.Pro307=
ENST00000642456.1:c.921A= ENSP00000493814.1:p.Pro307=
ENST00000643595.1:c.*725A= ENSP00000494497.1:n.*725A=
ENST00000644110.1:c.1008A= ENSP00000496392.1:p.Pro336=
ENST00000265849.11:c.1326A= ENSP00000265849.7:p.Pro442=
ENST00000382321.5:c.804-4448A= ENSP00000371758.4:n.804-4448A=
ENST00000406569.7:n.1326A=
ENST00000441476.6:c.1008A= ENSP00000392843.2:p.Pro336=
ENST00000469652.1:n.63-4534A=
NM_000535.5:c.1326A= , LRG_161t1:c.1326A= NP_000526.1:p.Pro442=
NR_003085.2:n.1408A=
XM_006715742.2:c.1320A= XP_006715805.1:p.Pro440=
XM_006715744.2:c.393A= XP_006715807.1:p.Pro131=
XM_011515427.1:c.1371A= XP_011513729.1:p.Pro457=
XM_011515428.1:c.1215A= XP_011513730.1:p.Pro405=
XM_011515429.1:c.1008A= XP_011513731.1:p.Pro336=
XM_011515430.1:c.1008A= XP_011513732.1:p.Pro336=
NM_000535.6:c.1326A= NP_000526.2:p.Pro442=
NM_001322003.1:c.921A= NP_001308932.1:p.Pro307=
NM_001322004.1:c.921A= NP_001308933.1:p.Pro307=
NM_001322005.1:c.921A= NP_001308934.1:p.Pro307=
NM_001322006.1:c.1170A= NP_001308935.1:p.Pro390=
NM_001322007.1:c.1008A= NP_001308936.1:p.Pro336=
NM_001322008.1:c.1008A= NP_001308937.1:p.Pro336=
NM_001322009.1:c.921A= NP_001308938.1:p.Pro307=
NM_001322010.1:c.765A= NP_001308939.1:p.Pro255=
NM_001322011.1:c.393A= NP_001308940.1:p.Pro131=
NM_001322012.1:c.393A= NP_001308941.1:p.Pro131=
NM_001322013.1:c.753A= NP_001308942.1:p.Pro251=
NM_001322014.1:c.1326A= NP_001308943.1:p.Pro442=
NM_001322015.1:c.1017A= NP_001308944.1:p.Pro339=
NR_136154.1:n.1413A=
XM_006715744.4:c.393A= XP_006715807.1:p.Pro131=
XM_017012342.2:c.393A= XP_016867831.1:p.Pro131=
XM_024446800.1:c.765A= XP_024302568.1:p.Pro255=
NM_000535.7:c.1326A= MANE Select NP_000526.2:p.Pro442=
NM_001322003.2:c.921A= NP_001308932.1:p.Pro307=
NM_001322004.2:c.921A= NP_001308933.1:p.Pro307=
NM_001322005.2:c.921A= NP_001308934.1:p.Pro307=
NM_001322006.2:c.1170A= NP_001308935.1:p.Pro390=
NM_001322008.2:c.1008A= NP_001308937.1:p.Pro336=
NM_001322009.2:c.921A= NP_001308938.1:p.Pro307=
NM_001322010.2:c.765A= NP_001308939.1:p.Pro255=
NM_001322011.2:c.393A= NP_001308940.1:p.Pro131=
NM_001322012.2:c.393A= NP_001308941.1:p.Pro131=
NM_001322013.2:c.753A= NP_001308942.1:p.Pro251=
NM_001322014.2:c.1326A= NP_001308943.1:p.Pro442=
NM_001322015.2:c.1017A= NP_001308944.1:p.Pro339=
NM_001322007.2:c.1008A= NP_001308936.1:p.Pro336=