Canonical Allele Identifier: CA2699317845

Gene: MSH2

Linked Data

• dbSNP Id: rs2104464590

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47483007_47483008insACTTTA , CM000664.2:g.47483007_47483008insACTTTA	GRCh38
NC_000002.11:g.47710146_47710147insACTTTA , CM000664.1:g.47710146_47710147insACTTTA	GRCh37
NC_000002.10:g.47563650_47563651insACTTTA	NCBI36
NG_007110.2:g.84884_84885insACTTTA , LRG_218:g.84884_84885insACTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634+2136_2634+2137insACTTTA	ENSP00000495641.2:n.2634+2136_2634+2137insACTTTA
ENST00000233146.7:c.*58_*59insACTTTA MANE Select	ENSP00000233146.2:n.*58_*59insACTTTA
ENST00000543555.6:c.*58_*59insACTTTA	ENSP00000442697.1:n.*58_*59insACTTTA
ENST00000644092.1:c.*934+2136_*934+2137insACTTTA	ENSP00000496351.1:n.*934+2136_*934+2137insACTTTA
ENST00000644900.1:c.487+2136_487+2137insACTTTA
ENST00000645339.1:c.2634+2136_2634+2137insACTTTA	ENSP00000496441.1:n.2634+2136_2634+2137insACTTTA
ENST00000645506.1:c.2634+2136_2634+2137insACTTTA	ENSP00000495455.1:n.2634+2136_2634+2137insACTTTA
ENST00000646415.1:c.2634+2136_2634+2137insACTTTA	ENSP00000495543.1:n.2634+2136_2634+2137insACTTTA
ENST00000233146.6:c.*58_*59insACTTTA	ENSP00000233146.2:n.*58_*59insACTTTA
ENST00000406134.5:c.2634+2136_2634+2137insACTTTA	ENSP00000384199.1:n.2634+2136_2634+2137insACTTTA
ENST00000461394.5:n.75+2136_75+2137insACTTTA
ENST00000543555.5:c.*58_*59insACTTTA	ENSP00000442697.1:n.*58_*59insACTTTA
ENST00000610696.4:c.*1259_*1260insACTTTA	ENSP00000483159.1:n.*1259_*1260insACTTTA
ENST00000613514.4:c.*1403_*1404insACTTTA	ENSP00000484137.1:n.*1403_*1404insACTTTA
ENST00000617333.3:c.*1629_*1630insACTTTA	ENSP00000482468.1:n.*1629_*1630insACTTTA
ENST00000617938.4:c.*1835_*1836insACTTTA	ENSP00000481158.1:n.*1835_*1836insACTTTA
ENST00000621359.2:c.*429_*430insACTTTA	ENSP00000481416.1:n.*429_*430insACTTTA
NM_000251.2:c.*58_*59insACTTTA , LRG_218t1:c.*58_*59insACTTTA	NP_000242.1:n.*58_*59insACTTTA
NM_001258281.1:c.*58_*59insACTTTA	NP_001245210.1:n.*58_*59insACTTTA
XM_005264332.2:c.2634+2136_2634+2137insACTTTA	XP_005264389.2:n.2634+2136_2634+2137insACTTTA
XM_011532867.1:c.2634+2136_2634+2137insACTTTA	XP_011531169.1:n.2634+2136_2634+2137insACTTTA
XR_939685.1:n.2706+2136_2706+2137insACTTTA
XM_005264332.4:c.2634+2136_2634+2137insACTTTA	XP_005264389.2:n.2634+2136_2634+2137insACTTTA
XM_011532867.2:c.2634+2136_2634+2137insACTTTA	XP_011531169.1:n.2634+2136_2634+2137insACTTTA
XR_001738747.2:n.2696+2136_2696+2137insACTTTA
XR_939685.2:n.2696+2136_2696+2137insACTTTA
NM_000251.3:c.*58_*59insACTTTA MANE Select	NP_000242.1:n.*58_*59insACTTTA