Canonical Allele Identifier: CA366735993
Gene: PMS2 HGNC NCBI

Linked Data

dbSNP Id: rs2128674952

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5977710T>A , CM000669.2:g.5977710T>A GRCh38
NC_000007.13:g.6017341T>A , CM000669.1:g.6017341T>A GRCh37
NC_000007.12:g.5983867T>A NCBI36
NG_008466.1:g.36397A>T , LRG_161:g.36397A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699814.2:c.*1719A>T ENSP00000514615.2:n.*1719A>T
ENST00000699840.2:c.2320A>T ENSP00000514638.2:p.Asn774Tyr
ENST00000699930.2:c.2215A>T ENSP00000514695.2:p.Asn739Tyr
ENST00000406569.8:c.1683A>T ENSP00000514464.1:p.Lys561Asn
ENST00000644110.2:c.*1917A>T ENSP00000496392.2:n.*1917A>T
ENST00000699752.1:c.2167A>T ENSP00000514561.1:p.Asn723Tyr
ENST00000699753.1:c.*1744A>T ENSP00000514562.1:n.*1744A>T
ENST00000699754.1:c.2125A>T ENSP00000514563.1:p.Asn709Tyr
ENST00000699755.1:c.*1722A>T ENSP00000514564.1:n.*1722A>T
ENST00000699756.1:c.*1910A>T ENSP00000514565.1:n.*1910A>T
ENST00000699757.1:c.*1580A>T ENSP00000514566.1:n.*1580A>T
ENST00000699758.1:c.*1580A>T ENSP00000514567.1:n.*1580A>T
ENST00000699759.1:n.3177A>T
ENST00000699760.1:c.2005A>T ENSP00000514568.1:p.Asn669Tyr
ENST00000699761.1:c.1918A>T ENSP00000514569.1:p.Asn640Tyr
ENST00000699762.1:c.1750A>T ENSP00000514570.1:p.Asn584Tyr
ENST00000699763.1:c.*1413A>T ENSP00000514571.1:n.*1413A>T
ENST00000699764.1:c.*641A>T ENSP00000514572.1:n.*641A>T
ENST00000699765.1:c.*1318A>T ENSP00000514573.1:n.*1318A>T
ENST00000699766.1:c.2356A>T ENSP00000514574.1:p.Asn786Tyr
ENST00000699767.1:c.2280A>T ENSP00000514575.1:p.Lys760Asn
ENST00000699768.1:c.2179A>T ENSP00000514576.1:p.Asn727Tyr
ENST00000699811.1:c.1918A>T ENSP00000514614.1:p.Asn640Tyr
ENST00000699813.1:n.2436A>T
ENST00000699814.1:c.1946A>T
ENST00000699815.1:c.*1854A>T ENSP00000514616.1:n.*1854A>T
ENST00000699816.1:c.*1213A>T ENSP00000514617.1:n.*1213A>T
ENST00000699817.1:c.*1917A>T ENSP00000514618.1:n.*1917A>T
ENST00000699818.1:c.1918A>T ENSP00000514619.1:p.Asn640Tyr
ENST00000699819.1:c.*1480A>T ENSP00000514620.1:n.*1480A>T
ENST00000699820.1:c.*261A>T ENSP00000514621.1:n.*261A>T
ENST00000699821.1:c.1951A>T ENSP00000514622.1:p.Asn651Tyr
ENST00000699822.1:c.*1775A>T ENSP00000514623.1:n.*1775A>T
ENST00000699823.1:c.1918A>T ENSP00000514624.1:p.Asn640Tyr
ENST00000699824.1:c.*1826A>T ENSP00000514625.1:n.*1826A>T
ENST00000699825.1:c.1762A>T ENSP00000514626.1:p.Asn588Tyr
ENST00000699826.1:c.*1722A>T ENSP00000514627.1:n.*1722A>T
ENST00000699827.1:c.2155A>T ENSP00000514628.1:p.Asn719Tyr
ENST00000699828.1:c.*1413A>T ENSP00000514629.1:n.*1413A>T
ENST00000699833.1:n.4095A>T
ENST00000699837.1:c.1918A>T ENSP00000514635.1:p.Asn640Tyr
ENST00000699838.1:c.*2223A>T ENSP00000514636.1:n.*2223A>T
ENST00000699839.1:c.2509A>T ENSP00000514637.1:p.Asn837Tyr
ENST00000699916.1:c.*1580A>T ENSP00000514684.1:n.*1580A>T
ENST00000699917.1:c.*1772A>T ENSP00000514685.1:n.*1772A>T
ENST00000699918.1:c.*1824A>T ENSP00000514686.1:n.*1824A>T
ENST00000699919.1:c.*1910A>T ENSP00000514687.1:n.*1910A>T
ENST00000699920.1:c.*1959A>T ENSP00000514688.1:n.*1959A>T
ENST00000699928.1:c.*261A>T ENSP00000514693.1:n.*261A>T
ENST00000699951.1:c.*1376A>T ENSP00000514706.1:n.*1376A>T
ENST00000699952.1:c.804-4168A>T ENSP00000514707.1:n.804-4168A>T
ENST00000265849.12:c.2323A>T MANE Select ENSP00000265849.7:p.Asn775Tyr
ENST00000642292.1:c.1918A>T ENSP00000495524.1:p.Asn640Tyr
ENST00000642456.1:c.1918A>T ENSP00000493814.1:p.Asn640Tyr
ENST00000643595.1:c.*1722A>T ENSP00000494497.1:n.*1722A>T
ENST00000644110.1:c.2005A>T ENSP00000496392.1:p.Asn669Tyr
ENST00000265849.11:c.2323A>T ENSP00000265849.7:p.Asn775Tyr
ENST00000382321.5:c.1120A>T ENSP00000371758.4:p.Asn374Tyr
ENST00000406569.7:n.1683A>T
ENST00000441476.6:c.2005A>T ENSP00000392843.2:p.Asn669Tyr
NM_000535.5:c.2323A>T , LRG_161t1:c.2323A>T NP_000526.1:p.Asn775Tyr
NR_003085.2:n.2405A>T
XM_006715742.2:c.2317A>T XP_006715805.1:p.Asn773Tyr
XM_006715744.2:c.1390A>T XP_006715807.1:p.Asn464Tyr
XM_011515427.1:c.2368A>T XP_011513729.1:p.Asn790Tyr
XM_011515428.1:c.2212A>T XP_011513730.1:p.Asn738Tyr
XM_011515429.1:c.2005A>T XP_011513731.1:p.Asn669Tyr
XM_011515430.1:c.2005A>T XP_011513732.1:p.Asn669Tyr
NM_000535.6:c.2323A>T NP_000526.2:p.Asn775Tyr
NM_001322003.1:c.1918A>T NP_001308932.1:p.Asn640Tyr
NM_001322004.1:c.1918A>T NP_001308933.1:p.Asn640Tyr
NM_001322005.1:c.1918A>T NP_001308934.1:p.Asn640Tyr
NM_001322006.1:c.2167A>T NP_001308935.1:p.Asn723Tyr
NM_001322007.1:c.2005A>T NP_001308936.1:p.Asn669Tyr
NM_001322008.1:c.2005A>T NP_001308937.1:p.Asn669Tyr
NM_001322009.1:c.1951A>T NP_001308938.1:p.Asn651Tyr
NM_001322010.1:c.1762A>T NP_001308939.1:p.Asn588Tyr
NM_001322011.1:c.1390A>T NP_001308940.1:p.Asn464Tyr
NM_001322012.1:c.1390A>T NP_001308941.1:p.Asn464Tyr
NM_001322013.1:c.1750A>T NP_001308942.1:p.Asn584Tyr
NM_001322014.1:c.2356A>T NP_001308943.1:p.Asn786Tyr
NM_001322015.1:c.2014A>T NP_001308944.1:p.Asn672Tyr
NR_136154.1:n.2367A>T
XM_006715744.4:c.1390A>T XP_006715807.1:p.Asn464Tyr
XM_017012342.2:c.1390A>T XP_016867831.1:p.Asn464Tyr
XM_024446800.1:c.1762A>T XP_024302568.1:p.Asn588Tyr
NM_000535.7:c.2323A>T MANE Select NP_000526.2:p.Asn775Tyr
NM_001322003.2:c.1918A>T NP_001308932.1:p.Asn640Tyr
NM_001322004.2:c.1918A>T NP_001308933.1:p.Asn640Tyr
NM_001322005.2:c.1918A>T NP_001308934.1:p.Asn640Tyr
NM_001322006.2:c.2167A>T NP_001308935.1:p.Asn723Tyr
NM_001322008.2:c.2005A>T NP_001308937.1:p.Asn669Tyr
NM_001322009.2:c.1951A>T NP_001308938.1:p.Asn651Tyr
NM_001322010.2:c.1762A>T NP_001308939.1:p.Asn588Tyr
NM_001322011.2:c.1390A>T NP_001308940.1:p.Asn464Tyr
NM_001322012.2:c.1390A>T NP_001308941.1:p.Asn464Tyr
NM_001322013.2:c.1750A>T NP_001308942.1:p.Asn584Tyr
NM_001322014.2:c.2356A>T NP_001308943.1:p.Asn786Tyr
NM_001322015.2:c.2014A>T NP_001308944.1:p.Asn672Tyr
NM_001322007.2:c.2005A>T NP_001308936.1:p.Asn669Tyr