Canonical Allele Identifier: CA2495876183

Gene: MSH2

Linked Data

• dbSNP Id: rs1667506177

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47480883_47480884insA , CM000664.2:g.47480883_47480884insA	GRCh38
NC_000002.11:g.47708022_47708023insA , CM000664.1:g.47708022_47708023insA	GRCh37
NC_000002.10:g.47561526_47561527insA	NCBI36
NG_007110.2:g.82760_82761insA , LRG_218:g.82760_82761insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634+12_2634+13insA	ENSP00000495641.2:n.2634+12_2634+13insA
ENST00000233146.7:c.2634+12_2634+13insA MANE Select	ENSP00000233146.2:n.2634+12_2634+13insA
ENST00000543555.6:c.2436+12_2436+13insA	ENSP00000442697.1:n.2436+12_2436+13insA
ENST00000644092.1:c.*934+12_*934+13insA	ENSP00000496351.1:n.*934+12_*934+13insA
ENST00000644900.1:c.487+12_487+13insA
ENST00000645339.1:c.2634+12_2634+13insA	ENSP00000496441.1:n.2634+12_2634+13insA
ENST00000645506.1:c.2634+12_2634+13insA	ENSP00000495455.1:n.2634+12_2634+13insA
ENST00000646415.1:c.2634+12_2634+13insA	ENSP00000495543.1:n.2634+12_2634+13insA
ENST00000233146.6:c.2634+12_2634+13insA	ENSP00000233146.2:n.2634+12_2634+13insA
ENST00000406134.5:c.2634+12_2634+13insA	ENSP00000384199.1:n.2634+12_2634+13insA
ENST00000461394.5:n.75+12_75+13insA
ENST00000543555.5:c.2436+12_2436+13insA	ENSP00000442697.1:n.2436+12_2436+13insA
ENST00000610696.4:c.*1030+12_*1030+13insA	ENSP00000483159.1:n.*1030+12_*1030+13insA
ENST00000613514.4:c.*1174+12_*1174+13insA	ENSP00000484137.1:n.*1174+12_*1174+13insA
ENST00000617333.3:c.*1400+12_*1400+13insA	ENSP00000482468.1:n.*1400+12_*1400+13insA
ENST00000617938.4:c.*1606+12_*1606+13insA	ENSP00000481158.1:n.*1606+12_*1606+13insA
ENST00000621359.2:c.*200+12_*200+13insA	ENSP00000481416.1:n.*200+12_*200+13insA
NM_000251.2:c.2634+12_2634+13insA , LRG_218t1:c.2634+12_2634+13insA	NP_000242.1:n.2634+12_2634+13insA
NM_001258281.1:c.2436+12_2436+13insA	NP_001245210.1:n.2436+12_2436+13insA
XM_005264332.2:c.2634+12_2634+13insA	XP_005264389.2:n.2634+12_2634+13insA
XM_011532867.1:c.2634+12_2634+13insA	XP_011531169.1:n.2634+12_2634+13insA
XR_939685.1:n.2706+12_2706+13insA
XM_005264332.4:c.2634+12_2634+13insA	XP_005264389.2:n.2634+12_2634+13insA
XM_011532867.2:c.2634+12_2634+13insA	XP_011531169.1:n.2634+12_2634+13insA
XR_001738747.2:n.2696+12_2696+13insA
XR_939685.2:n.2696+12_2696+13insA
NM_000251.3:c.2634+12_2634+13insA MANE Select	NP_000242.1:n.2634+12_2634+13insA