Canonical Allele Identifier: CA366737997
Gene: PMS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5982898C>A , CM000669.2:g.5982898C>A GRCh38
NC_000007.13:g.6022529C>A , CM000669.1:g.6022529C>A GRCh37
NC_000007.12:g.5989055C>A NCBI36
NG_008466.1:g.31209G>T , LRG_161:g.31209G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000699814.2:c.*1496G>T ENSP00000514615.2:n.*1496G>T
ENST00000699840.2:c.2097G>T ENSP00000514638.2:p.Gln699His
ENST00000699930.2:c.1992G>T ENSP00000514695.2:p.Gln664His
ENST00000406569.8:c.1678+4189G>T ENSP00000514464.1:n.1678+4189G>T
ENST00000644110.2:c.*1694G>T ENSP00000496392.2:n.*1694G>T
ENST00000699752.1:c.1944G>T ENSP00000514561.1:p.Gln648His
ENST00000699753.1:c.*1521G>T ENSP00000514562.1:n.*1521G>T
ENST00000699754.1:c.1902G>T ENSP00000514563.1:p.Gln634His
ENST00000699755.1:c.*1499G>T ENSP00000514564.1:n.*1499G>T
ENST00000699756.1:c.*1687G>T ENSP00000514565.1:n.*1687G>T
ENST00000699757.1:c.*1357G>T ENSP00000514566.1:n.*1357G>T
ENST00000699758.1:c.*1357G>T ENSP00000514567.1:n.*1357G>T
ENST00000699759.1:n.2954G>T
ENST00000699760.1:c.1782G>T ENSP00000514568.1:p.Gln594His
ENST00000699761.1:c.1695G>T ENSP00000514569.1:p.Gln565His
ENST00000699762.1:c.1527G>T ENSP00000514570.1:p.Gln509His
ENST00000699763.1:c.*1190G>T ENSP00000514571.1:n.*1190G>T
ENST00000699764.1:c.*418G>T ENSP00000514572.1:n.*418G>T
ENST00000699765.1:c.*1196G>T ENSP00000514573.1:n.*1196G>T
ENST00000699766.1:c.2100G>T ENSP00000514574.1:p.Gln700His
ENST00000699767.1:c.2100G>T ENSP00000514575.1:p.Gln700His
ENST00000699768.1:c.2100G>T ENSP00000514576.1:p.Gln700His
ENST00000699811.1:c.1695G>T ENSP00000514614.1:p.Gln565His
ENST00000699813.1:n.2213G>T
ENST00000699814.1:c.1723G>T
ENST00000699815.1:c.*1631G>T ENSP00000514616.1:n.*1631G>T
ENST00000699816.1:c.*990G>T ENSP00000514617.1:n.*990G>T
ENST00000699817.1:c.*1694G>T ENSP00000514618.1:n.*1694G>T
ENST00000699818.1:c.1695G>T ENSP00000514619.1:p.Gln565His
ENST00000699819.1:c.*1257G>T ENSP00000514620.1:n.*1257G>T
ENST00000699820.1:c.*38G>T ENSP00000514621.1:n.*38G>T
ENST00000699821.1:c.1695G>T ENSP00000514622.1:p.Gln565His
ENST00000699822.1:c.*1552G>T ENSP00000514623.1:n.*1552G>T
ENST00000699823.1:c.1695G>T ENSP00000514624.1:p.Gln565His
ENST00000699824.1:c.*1603G>T ENSP00000514625.1:n.*1603G>T
ENST00000699825.1:c.1539G>T ENSP00000514626.1:p.Gln513His
ENST00000699826.1:c.*1499G>T ENSP00000514627.1:n.*1499G>T
ENST00000699827.1:c.1932G>T ENSP00000514628.1:p.Gln644His
ENST00000699828.1:c.*1190G>T ENSP00000514629.1:n.*1190G>T
ENST00000699833.1:n.3872G>T
ENST00000699837.1:c.1695G>T ENSP00000514635.1:p.Gln565His
ENST00000699838.1:c.*2000G>T ENSP00000514636.1:n.*2000G>T
ENST00000699839.1:c.2286G>T ENSP00000514637.1:p.Gln762His
ENST00000699916.1:c.*1357G>T ENSP00000514684.1:n.*1357G>T
ENST00000699917.1:c.*1549G>T ENSP00000514685.1:n.*1549G>T
ENST00000699918.1:c.*1601G>T ENSP00000514686.1:n.*1601G>T
ENST00000699919.1:c.*1687G>T ENSP00000514687.1:n.*1687G>T
ENST00000699920.1:c.*1736G>T ENSP00000514688.1:n.*1736G>T
ENST00000699928.1:c.*38G>T ENSP00000514693.1:n.*38G>T
ENST00000699951.1:c.*1196G>T ENSP00000514706.1:n.*1196G>T
ENST00000699952.1:c.804-9356G>T ENSP00000514707.1:n.804-9356G>T
ENST00000265849.12:c.2100G>T MANE Select ENSP00000265849.7:p.Gln700His
ENST00000642292.1:c.1695G>T ENSP00000495524.1:p.Gln565His
ENST00000642456.1:c.1695G>T ENSP00000493814.1:p.Gln565His
ENST00000643595.1:c.*1499G>T ENSP00000494497.1:n.*1499G>T
ENST00000644110.1:c.1782G>T ENSP00000496392.1:p.Gln594His
ENST00000265849.11:c.2100G>T ENSP00000265849.7:p.Gln700His
ENST00000382321.5:c.897G>T ENSP00000371758.4:p.Gln299His
ENST00000406569.7:n.1678+4189G>T
ENST00000441476.6:c.1782G>T ENSP00000392843.2:p.Gln594His
ENST00000469652.1:n.70G>T
NM_000535.5:c.2100G>T , LRG_161t1:c.2100G>T NP_000526.1:p.Gln700His
NR_003085.2:n.2182G>T
XM_006715742.2:c.2094G>T XP_006715805.1:p.Gln698His
XM_006715744.2:c.1167G>T XP_006715807.1:p.Gln389His
XM_011515427.1:c.2145G>T XP_011513729.1:p.Gln715His
XM_011515428.1:c.1989G>T XP_011513730.1:p.Gln663His
XM_011515429.1:c.1782G>T XP_011513731.1:p.Gln594His
XM_011515430.1:c.1782G>T XP_011513732.1:p.Gln594His
NM_000535.6:c.2100G>T NP_000526.2:p.Gln700His
NM_001322003.1:c.1695G>T NP_001308932.1:p.Gln565His
NM_001322004.1:c.1695G>T NP_001308933.1:p.Gln565His
NM_001322005.1:c.1695G>T NP_001308934.1:p.Gln565His
NM_001322006.1:c.1944G>T NP_001308935.1:p.Gln648His
NM_001322007.1:c.1782G>T NP_001308936.1:p.Gln594His
NM_001322008.1:c.1782G>T NP_001308937.1:p.Gln594His
NM_001322009.1:c.1695G>T NP_001308938.1:p.Gln565His
NM_001322010.1:c.1539G>T NP_001308939.1:p.Gln513His
NM_001322011.1:c.1167G>T NP_001308940.1:p.Gln389His
NM_001322012.1:c.1167G>T NP_001308941.1:p.Gln389His
NM_001322013.1:c.1527G>T NP_001308942.1:p.Gln509His
NM_001322014.1:c.2100G>T NP_001308943.1:p.Gln700His
NM_001322015.1:c.1791G>T NP_001308944.1:p.Gln597His
NR_136154.1:n.2187G>T
XM_006715744.4:c.1167G>T XP_006715807.1:p.Gln389His
XM_017012342.2:c.1167G>T XP_016867831.1:p.Gln389His
XM_024446800.1:c.1539G>T XP_024302568.1:p.Gln513His
NM_000535.7:c.2100G>T MANE Select NP_000526.2:p.Gln700His
NM_001322003.2:c.1695G>T NP_001308932.1:p.Gln565His
NM_001322004.2:c.1695G>T NP_001308933.1:p.Gln565His
NM_001322005.2:c.1695G>T NP_001308934.1:p.Gln565His
NM_001322006.2:c.1944G>T NP_001308935.1:p.Gln648His
NM_001322008.2:c.1782G>T NP_001308937.1:p.Gln594His
NM_001322009.2:c.1695G>T NP_001308938.1:p.Gln565His
NM_001322010.2:c.1539G>T NP_001308939.1:p.Gln513His
NM_001322011.2:c.1167G>T NP_001308940.1:p.Gln389His
NM_001322012.2:c.1167G>T NP_001308941.1:p.Gln389His
NM_001322013.2:c.1527G>T NP_001308942.1:p.Gln509His
NM_001322014.2:c.2100G>T NP_001308943.1:p.Gln700His
NM_001322015.2:c.1791G>T NP_001308944.1:p.Gln597His
NM_001322007.2:c.1782G>T NP_001308936.1:p.Gln594His