Canonical Allele Identifier: CA366735721
Gene: PMS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 663981
ClinVar RCV Id: RCV000821967
dbSNP Id: rs267608152

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5977643A>T , CM000669.2:g.5977643A>T GRCh38
NC_000007.13:g.6017274A>T , CM000669.1:g.6017274A>T GRCh37
NC_000007.12:g.5983800A>T NCBI36
NG_008466.1:g.36464T>A , LRG_161:g.36464T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699814.2:c.*1786T>A ENSP00000514615.2:n.*1786T>A
ENST00000699840.2:c.2387T>A ENSP00000514638.2:p.Met796Lys
ENST00000699930.2:c.2282T>A ENSP00000514695.2:p.Met761Lys
ENST00000406569.8:c.1750T>A ENSP00000514464.1:n.1750T>A
ENST00000644110.2:c.*1984T>A ENSP00000496392.2:n.*1984T>A
ENST00000699752.1:c.2234T>A ENSP00000514561.1:p.Met745Lys
ENST00000699753.1:c.*1811T>A ENSP00000514562.1:n.*1811T>A
ENST00000699754.1:c.2192T>A ENSP00000514563.1:p.Met731Lys
ENST00000699755.1:c.*1789T>A ENSP00000514564.1:n.*1789T>A
ENST00000699756.1:c.*1977T>A ENSP00000514565.1:n.*1977T>A
ENST00000699757.1:c.*1647T>A ENSP00000514566.1:n.*1647T>A
ENST00000699758.1:c.*1647T>A ENSP00000514567.1:n.*1647T>A
ENST00000699759.1:n.3244T>A
ENST00000699760.1:c.2072T>A ENSP00000514568.1:p.Met691Lys
ENST00000699761.1:c.1985T>A ENSP00000514569.1:p.Met662Lys
ENST00000699762.1:c.1817T>A ENSP00000514570.1:p.Met606Lys
ENST00000699763.1:c.*1480T>A ENSP00000514571.1:n.*1480T>A
ENST00000699764.1:c.*708T>A ENSP00000514572.1:n.*708T>A
ENST00000699765.1:c.*1385T>A ENSP00000514573.1:n.*1385T>A
ENST00000699766.1:c.2423T>A ENSP00000514574.1:p.Met808Lys
ENST00000699767.1:c.*31T>A ENSP00000514575.1:n.*31T>A
ENST00000699768.1:c.2246T>A ENSP00000514576.1:p.Met749Lys
ENST00000699811.1:c.1985T>A ENSP00000514614.1:p.Met662Lys
ENST00000699813.1:n.2503T>A
ENST00000699814.1:c.2013T>A
ENST00000699815.1:c.*1921T>A ENSP00000514616.1:n.*1921T>A
ENST00000699816.1:c.*1280T>A ENSP00000514617.1:n.*1280T>A
ENST00000699817.1:c.*1984T>A ENSP00000514618.1:n.*1984T>A
ENST00000699818.1:c.1985T>A ENSP00000514619.1:p.Met662Lys
ENST00000699819.1:c.*1547T>A ENSP00000514620.1:n.*1547T>A
ENST00000699820.1:c.*328T>A ENSP00000514621.1:n.*328T>A
ENST00000699821.1:c.2018T>A ENSP00000514622.1:p.Met673Lys
ENST00000699822.1:c.*1842T>A ENSP00000514623.1:n.*1842T>A
ENST00000699823.1:c.1985T>A ENSP00000514624.1:p.Met662Lys
ENST00000699824.1:c.*1893T>A ENSP00000514625.1:n.*1893T>A
ENST00000699825.1:c.1829T>A ENSP00000514626.1:p.Met610Lys
ENST00000699826.1:c.*1789T>A ENSP00000514627.1:n.*1789T>A
ENST00000699827.1:c.2222T>A ENSP00000514628.1:p.Met741Lys
ENST00000699828.1:c.*1480T>A ENSP00000514629.1:n.*1480T>A
ENST00000699833.1:n.4162T>A
ENST00000699837.1:c.1985T>A ENSP00000514635.1:p.Met662Lys
ENST00000699838.1:c.*2290T>A ENSP00000514636.1:n.*2290T>A
ENST00000699839.1:c.2576T>A ENSP00000514637.1:p.Met859Lys
ENST00000699916.1:c.*1647T>A ENSP00000514684.1:n.*1647T>A
ENST00000699917.1:c.*1839T>A ENSP00000514685.1:n.*1839T>A
ENST00000699918.1:c.*1891T>A ENSP00000514686.1:n.*1891T>A
ENST00000699919.1:c.*1977T>A ENSP00000514687.1:n.*1977T>A
ENST00000699920.1:c.*2026T>A ENSP00000514688.1:n.*2026T>A
ENST00000699928.1:c.*328T>A ENSP00000514693.1:n.*328T>A
ENST00000699951.1:c.*1443T>A ENSP00000514706.1:n.*1443T>A
ENST00000699952.1:c.804-4101T>A ENSP00000514707.1:n.804-4101T>A
ENST00000265849.12:c.2390T>A MANE Select ENSP00000265849.7:p.Met797Lys
ENST00000642292.1:c.1985T>A ENSP00000495524.1:p.Met662Lys
ENST00000642456.1:c.1985T>A ENSP00000493814.1:p.Met662Lys
ENST00000643595.1:c.*1789T>A ENSP00000494497.1:n.*1789T>A
ENST00000644110.1:c.2072T>A ENSP00000496392.1:p.Met691Lys
ENST00000265849.11:c.2390T>A ENSP00000265849.7:p.Met797Lys
ENST00000382321.5:c.1187T>A ENSP00000371758.4:p.Met396Lys
ENST00000441476.6:c.2072T>A ENSP00000392843.2:p.Met691Lys
NM_000535.5:c.2390T>A , LRG_161t1:c.2390T>A NP_000526.1:p.Met797Lys
NR_003085.2:n.2472T>A
XM_006715742.2:c.2384T>A XP_006715805.1:p.Met795Lys
XM_006715744.2:c.1457T>A XP_006715807.1:p.Met486Lys
XM_011515427.1:c.2435T>A XP_011513729.1:p.Met812Lys
XM_011515428.1:c.2279T>A XP_011513730.1:p.Met760Lys
XM_011515429.1:c.2072T>A XP_011513731.1:p.Met691Lys
XM_011515430.1:c.2072T>A XP_011513732.1:p.Met691Lys
NM_000535.6:c.2390T>A NP_000526.2:p.Met797Lys
NM_001322003.1:c.1985T>A NP_001308932.1:p.Met662Lys
NM_001322004.1:c.1985T>A NP_001308933.1:p.Met662Lys
NM_001322005.1:c.1985T>A NP_001308934.1:p.Met662Lys
NM_001322006.1:c.2234T>A NP_001308935.1:p.Met745Lys
NM_001322007.1:c.2072T>A NP_001308936.1:p.Met691Lys
NM_001322008.1:c.2072T>A NP_001308937.1:p.Met691Lys
NM_001322009.1:c.2018T>A NP_001308938.1:p.Met673Lys
NM_001322010.1:c.1829T>A NP_001308939.1:p.Met610Lys
NM_001322011.1:c.1457T>A NP_001308940.1:p.Met486Lys
NM_001322012.1:c.1457T>A NP_001308941.1:p.Met486Lys
NM_001322013.1:c.1817T>A NP_001308942.1:p.Met606Lys
NM_001322014.1:c.2423T>A NP_001308943.1:p.Met808Lys
NM_001322015.1:c.2081T>A NP_001308944.1:p.Met694Lys
NR_136154.1:n.2434T>A
XM_006715744.4:c.1457T>A XP_006715807.1:p.Met486Lys
XM_017012342.2:c.1457T>A XP_016867831.1:p.Met486Lys
XM_024446800.1:c.1829T>A XP_024302568.1:p.Met610Lys
NM_000535.7:c.2390T>A MANE Select NP_000526.2:p.Met797Lys
NM_001322003.2:c.1985T>A NP_001308932.1:p.Met662Lys
NM_001322004.2:c.1985T>A NP_001308933.1:p.Met662Lys
NM_001322005.2:c.1985T>A NP_001308934.1:p.Met662Lys
NM_001322006.2:c.2234T>A NP_001308935.1:p.Met745Lys
NM_001322008.2:c.2072T>A NP_001308937.1:p.Met691Lys
NM_001322009.2:c.2018T>A NP_001308938.1:p.Met673Lys
NM_001322010.2:c.1829T>A NP_001308939.1:p.Met610Lys
NM_001322011.2:c.1457T>A NP_001308940.1:p.Met486Lys
NM_001322012.2:c.1457T>A NP_001308941.1:p.Met486Lys
NM_001322013.2:c.1817T>A NP_001308942.1:p.Met606Lys
NM_001322014.2:c.2423T>A NP_001308943.1:p.Met808Lys
NM_001322015.2:c.2081T>A NP_001308944.1:p.Met694Lys
NM_001322007.2:c.2072T>A NP_001308936.1:p.Met691Lys