Canonical Allele Identifier: CA366734727
Gene: PMS2 HGNC NCBI

Linked Data

dbSNP Id: rs2128656703

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5973412A>C , CM000669.2:g.5973412A>C GRCh38
NC_000007.13:g.6013043A>C , CM000669.1:g.6013043A>C GRCh37
NC_000007.12:g.5979569A>C NCBI36
NG_008466.1:g.40695T>G , LRG_161:g.40695T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699814.2:c.*1972T>G ENSP00000514615.2:n.*1972T>G
ENST00000699840.2:c.2573T>G ENSP00000514638.2:p.Ile858Ser
ENST00000699930.2:c.2468T>G ENSP00000514695.2:p.Ile823Ser
ENST00000406569.8:c.1936T>G ENSP00000514464.1:n.1936T>G
ENST00000644110.2:c.*2170T>G ENSP00000496392.2:n.*2170T>G
ENST00000699752.1:c.2420T>G ENSP00000514561.1:p.Ile807Ser
ENST00000699753.1:c.*1997T>G ENSP00000514562.1:n.*1997T>G
ENST00000699754.1:c.2378T>G ENSP00000514563.1:p.Ile793Ser
ENST00000699755.1:c.*1975T>G ENSP00000514564.1:n.*1975T>G
ENST00000699756.1:c.*2163T>G ENSP00000514565.1:n.*2163T>G
ENST00000699757.1:c.*1833T>G ENSP00000514566.1:n.*1833T>G
ENST00000699758.1:c.*1833T>G ENSP00000514567.1:n.*1833T>G
ENST00000699759.1:n.3430T>G
ENST00000699760.1:c.2258T>G ENSP00000514568.1:p.Ile753Ser
ENST00000699761.1:c.2171T>G ENSP00000514569.1:p.Ile724Ser
ENST00000699762.1:c.2003T>G ENSP00000514570.1:p.Ile668Ser
ENST00000699763.1:c.*1666T>G ENSP00000514571.1:n.*1666T>G
ENST00000699764.1:c.*894T>G ENSP00000514572.1:n.*894T>G
ENST00000699765.1:c.*1571T>G ENSP00000514573.1:n.*1571T>G
ENST00000699766.1:c.2609T>G ENSP00000514574.1:p.Ile870Ser
ENST00000699767.1:c.*217T>G ENSP00000514575.1:n.*217T>G
ENST00000699768.1:c.2432T>G ENSP00000514576.1:p.Ile811Ser
ENST00000699811.1:c.2171T>G ENSP00000514614.1:p.Ile724Ser
ENST00000699813.1:n.2689T>G
ENST00000699814.1:c.2199T>G
ENST00000699815.1:c.*2107T>G ENSP00000514616.1:n.*2107T>G
ENST00000699816.1:c.*1466T>G ENSP00000514617.1:n.*1466T>G
ENST00000699817.1:c.*2170T>G ENSP00000514618.1:n.*2170T>G
ENST00000699818.1:c.2171T>G ENSP00000514619.1:p.Ile724Ser
ENST00000699819.1:c.*1733T>G ENSP00000514620.1:n.*1733T>G
ENST00000699820.1:c.*514T>G ENSP00000514621.1:n.*514T>G
ENST00000699821.1:c.2204T>G ENSP00000514622.1:p.Ile735Ser
ENST00000699822.1:c.*2028T>G ENSP00000514623.1:n.*2028T>G
ENST00000699823.1:c.2171T>G ENSP00000514624.1:p.Ile724Ser
ENST00000699824.1:c.*2079T>G ENSP00000514625.1:n.*2079T>G
ENST00000699825.1:c.2015T>G ENSP00000514626.1:p.Ile672Ser
ENST00000699826.1:c.*1975T>G ENSP00000514627.1:n.*1975T>G
ENST00000699827.1:c.2408T>G ENSP00000514628.1:p.Ile803Ser
ENST00000699828.1:c.*1666T>G ENSP00000514629.1:n.*1666T>G
ENST00000699833.1:n.4348T>G
ENST00000699837.1:c.2171T>G ENSP00000514635.1:p.Ile724Ser
ENST00000699838.1:c.*2476T>G ENSP00000514636.1:n.*2476T>G
ENST00000699839.1:c.2762T>G ENSP00000514637.1:p.Ile921Ser
ENST00000699916.1:c.*1833T>G ENSP00000514684.1:n.*1833T>G
ENST00000699917.1:c.*2025T>G ENSP00000514685.1:n.*2025T>G
ENST00000699918.1:c.*2077T>G ENSP00000514686.1:n.*2077T>G
ENST00000699919.1:c.*2163T>G ENSP00000514687.1:n.*2163T>G
ENST00000699920.1:c.*2212T>G ENSP00000514688.1:n.*2212T>G
ENST00000699928.1:c.*514T>G ENSP00000514693.1:n.*514T>G
ENST00000699951.1:c.*1629T>G ENSP00000514706.1:n.*1629T>G
ENST00000699952.1:c.*130T>G ENSP00000514707.1:n.*130T>G
ENST00000265849.12:c.2576T>G MANE Select ENSP00000265849.7:p.Ile859Ser
ENST00000642292.1:c.2171T>G ENSP00000495524.1:p.Ile724Ser
ENST00000642456.1:c.2171T>G ENSP00000493814.1:p.Ile724Ser
ENST00000643595.1:c.*1975T>G ENSP00000494497.1:n.*1975T>G
ENST00000644110.1:c.2258T>G ENSP00000496392.1:p.Ile753Ser
ENST00000265849.11:c.2576T>G ENSP00000265849.7:p.Ile859Ser
ENST00000382321.5:c.1373T>G ENSP00000371758.4:p.Ile458Ser
ENST00000441476.6:c.2258T>G ENSP00000392843.2:p.Ile753Ser
NM_000535.5:c.2576T>G , LRG_161t1:c.2576T>G NP_000526.1:p.Ile859Ser
NR_003085.2:n.2658T>G
XM_006715742.2:c.2570T>G XP_006715805.1:p.Ile857Ser
XM_006715744.2:c.1643T>G XP_006715807.1:p.Ile548Ser
XM_011515427.1:c.2621T>G XP_011513729.1:p.Ile874Ser
XM_011515428.1:c.2465T>G XP_011513730.1:p.Ile822Ser
XM_011515429.1:c.2258T>G XP_011513731.1:p.Ile753Ser
XM_011515430.1:c.2258T>G XP_011513732.1:p.Ile753Ser
NM_000535.6:c.2576T>G NP_000526.2:p.Ile859Ser
NM_001322003.1:c.2171T>G NP_001308932.1:p.Ile724Ser
NM_001322004.1:c.2171T>G NP_001308933.1:p.Ile724Ser
NM_001322005.1:c.2171T>G NP_001308934.1:p.Ile724Ser
NM_001322006.1:c.2420T>G NP_001308935.1:p.Ile807Ser
NM_001322007.1:c.2258T>G NP_001308936.1:p.Ile753Ser
NM_001322008.1:c.2258T>G NP_001308937.1:p.Ile753Ser
NM_001322009.1:c.2204T>G NP_001308938.1:p.Ile735Ser
NM_001322010.1:c.2015T>G NP_001308939.1:p.Ile672Ser
NM_001322011.1:c.1643T>G NP_001308940.1:p.Ile548Ser
NM_001322012.1:c.1643T>G NP_001308941.1:p.Ile548Ser
NM_001322013.1:c.2003T>G NP_001308942.1:p.Ile668Ser
NM_001322014.1:c.2609T>G NP_001308943.1:p.Ile870Ser
NM_001322015.1:c.2267T>G NP_001308944.1:p.Ile756Ser
NR_136154.1:n.2620T>G
XM_006715744.4:c.1643T>G XP_006715807.1:p.Ile548Ser
XM_017012342.2:c.1643T>G XP_016867831.1:p.Ile548Ser
XM_024446800.1:c.2015T>G XP_024302568.1:p.Ile672Ser
NM_000535.7:c.2576T>G MANE Select NP_000526.2:p.Ile859Ser
NM_001322003.2:c.2171T>G NP_001308932.1:p.Ile724Ser
NM_001322004.2:c.2171T>G NP_001308933.1:p.Ile724Ser
NM_001322005.2:c.2171T>G NP_001308934.1:p.Ile724Ser
NM_001322006.2:c.2420T>G NP_001308935.1:p.Ile807Ser
NM_001322008.2:c.2258T>G NP_001308937.1:p.Ile753Ser
NM_001322009.2:c.2204T>G NP_001308938.1:p.Ile735Ser
NM_001322010.2:c.2015T>G NP_001308939.1:p.Ile672Ser
NM_001322011.2:c.1643T>G NP_001308940.1:p.Ile548Ser
NM_001322012.2:c.1643T>G NP_001308941.1:p.Ile548Ser
NM_001322013.2:c.2003T>G NP_001308942.1:p.Ile668Ser
NM_001322014.2:c.2609T>G NP_001308943.1:p.Ile870Ser
NM_001322015.2:c.2267T>G NP_001308944.1:p.Ile756Ser
NM_001322007.2:c.2258T>G NP_001308936.1:p.Ile753Ser