Canonical Allele Identifier: CA2495876203

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47480909_47480912delinsCTAT , CM000664.2:g.47480909_47480912delinsCTAT	GRCh38
NC_000002.11:g.47708048_47708051delinsCTAT , CM000664.1:g.47708048_47708051delinsCTAT	GRCh37
NC_000002.10:g.47561552_47561555delinsCTAT	NCBI36
NG_007110.2:g.82786_82789delinsCTAT , LRG_218:g.82786_82789delinsCTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634+38_2634+41delinsCTAT	ENSP00000495641.2:n.2634+38_2634+41delinsCTAT
ENST00000233146.7:c.2634+38_2634+41delinsCTAT MANE Select	ENSP00000233146.2:n.2634+38_2634+41delinsCTAT
ENST00000543555.6:c.2436+38_2436+41delinsCTAT	ENSP00000442697.1:n.2436+38_2436+41delinsCTAT
ENST00000644092.1:c.*934+38_*934+41delinsCTAT	ENSP00000496351.1:n.*934+38_*934+41delinsCTAT
ENST00000644900.1:c.487+38_487+41delinsCTAT
ENST00000645339.1:c.2634+38_2634+41delinsCTAT	ENSP00000496441.1:n.2634+38_2634+41delinsCTAT
ENST00000645506.1:c.2634+38_2634+41delinsCTAT	ENSP00000495455.1:n.2634+38_2634+41delinsCTAT
ENST00000646415.1:c.2634+38_2634+41delinsCTAT	ENSP00000495543.1:n.2634+38_2634+41delinsCTAT
ENST00000233146.6:c.2634+38_2634+41delinsCTAT	ENSP00000233146.2:n.2634+38_2634+41delinsCTAT
ENST00000406134.5:c.2634+38_2634+41delinsCTAT	ENSP00000384199.1:n.2634+38_2634+41delinsCTAT
ENST00000461394.5:n.75+38_75+41delinsCTAT
ENST00000543555.5:c.2436+38_2436+41delinsCTAT	ENSP00000442697.1:n.2436+38_2436+41delinsCTAT
ENST00000610696.4:c.*1030+38_*1030+41delinsCTAT	ENSP00000483159.1:n.*1030+38_*1030+41delinsCTAT
ENST00000613514.4:c.*1174+38_*1174+41delinsCTAT	ENSP00000484137.1:n.*1174+38_*1174+41delinsCTAT
ENST00000617333.3:c.*1400+38_*1400+41delinsCTAT	ENSP00000482468.1:n.*1400+38_*1400+41delinsCTAT
ENST00000617938.4:c.*1606+38_*1606+41delinsCTAT	ENSP00000481158.1:n.*1606+38_*1606+41delinsCTAT
ENST00000621359.2:c.*200+38_*200+41delinsCTAT	ENSP00000481416.1:n.*200+38_*200+41delinsCTAT
NM_000251.2:c.2634+38_2634+41delinsCTAT , LRG_218t1:c.2634+38_2634+41delinsCTAT	NP_000242.1:n.2634+38_2634+41delinsCTAT
NM_001258281.1:c.2436+38_2436+41delinsCTAT	NP_001245210.1:n.2436+38_2436+41delinsCTAT
XM_005264332.2:c.2634+38_2634+41delinsCTAT	XP_005264389.2:n.2634+38_2634+41delinsCTAT
XM_011532867.1:c.2634+38_2634+41delinsCTAT	XP_011531169.1:n.2634+38_2634+41delinsCTAT
XR_939685.1:n.2706+38_2706+41delinsCTAT
XM_005264332.4:c.2634+38_2634+41delinsCTAT	XP_005264389.2:n.2634+38_2634+41delinsCTAT
XM_011532867.2:c.2634+38_2634+41delinsCTAT	XP_011531169.1:n.2634+38_2634+41delinsCTAT
XR_001738747.2:n.2696+38_2696+41delinsCTAT
XR_939685.2:n.2696+38_2696+41delinsCTAT
NM_000251.3:c.2634+38_2634+41delinsCTAT MANE Select	NP_000242.1:n.2634+38_2634+41delinsCTAT