Canonical Allele Identifier: CA2495876304

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47481079_47481080delinsAG , CM000664.2:g.47481079_47481080delinsAG	GRCh38
NC_000002.11:g.47708218_47708219delinsAG , CM000664.1:g.47708218_47708219delinsAG	GRCh37
NC_000002.10:g.47561722_47561723delinsAG	NCBI36
NG_007110.2:g.82956_82957delinsAG , LRG_218:g.82956_82957delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634+208_2634+209delinsAG	ENSP00000495641.2:n.2634+208_2634+209delinsAG
ENST00000233146.7:c.2634+208_2634+209delinsAG MANE Select	ENSP00000233146.2:n.2634+208_2634+209delinsAG
ENST00000543555.6:c.2436+208_2436+209delinsAG	ENSP00000442697.1:n.2436+208_2436+209delinsAG
ENST00000644092.1:c.*934+208_*934+209delinsAG	ENSP00000496351.1:n.*934+208_*934+209delinsAG
ENST00000644900.1:c.487+208_487+209delinsAG
ENST00000645339.1:c.2634+208_2634+209delinsAG	ENSP00000496441.1:n.2634+208_2634+209delinsAG
ENST00000645506.1:c.2634+208_2634+209delinsAG	ENSP00000495455.1:n.2634+208_2634+209delinsAG
ENST00000646415.1:c.2634+208_2634+209delinsAG	ENSP00000495543.1:n.2634+208_2634+209delinsAG
ENST00000233146.6:c.2634+208_2634+209delinsAG	ENSP00000233146.2:n.2634+208_2634+209delinsAG
ENST00000406134.5:c.2634+208_2634+209delinsAG	ENSP00000384199.1:n.2634+208_2634+209delinsAG
ENST00000461394.5:n.75+208_75+209delinsAG
ENST00000543555.5:c.2436+208_2436+209delinsAG	ENSP00000442697.1:n.2436+208_2436+209delinsAG
ENST00000610696.4:c.*1030+208_*1030+209delinsAG	ENSP00000483159.1:n.*1030+208_*1030+209delinsAG
ENST00000613514.4:c.*1174+208_*1174+209delinsAG	ENSP00000484137.1:n.*1174+208_*1174+209delinsAG
ENST00000617333.3:c.*1400+208_*1400+209delinsAG	ENSP00000482468.1:n.*1400+208_*1400+209delinsAG
ENST00000617938.4:c.*1606+208_*1606+209delinsAG	ENSP00000481158.1:n.*1606+208_*1606+209delinsAG
ENST00000621359.2:c.*200+208_*200+209delinsAG	ENSP00000481416.1:n.*200+208_*200+209delinsAG
NM_000251.2:c.2634+208_2634+209delinsAG , LRG_218t1:c.2634+208_2634+209delinsAG	NP_000242.1:n.2634+208_2634+209delinsAG
NM_001258281.1:c.2436+208_2436+209delinsAG	NP_001245210.1:n.2436+208_2436+209delinsAG
XM_005264332.2:c.2634+208_2634+209delinsAG	XP_005264389.2:n.2634+208_2634+209delinsAG
XM_011532867.1:c.2634+208_2634+209delinsAG	XP_011531169.1:n.2634+208_2634+209delinsAG
XR_939685.1:n.2706+208_2706+209delinsAG
XM_005264332.4:c.2634+208_2634+209delinsAG	XP_005264389.2:n.2634+208_2634+209delinsAG
XM_011532867.2:c.2634+208_2634+209delinsAG	XP_011531169.1:n.2634+208_2634+209delinsAG
XR_001738747.2:n.2696+208_2696+209delinsAG
XR_939685.2:n.2696+208_2696+209delinsAG
NM_000251.3:c.2634+208_2634+209delinsAG MANE Select	NP_000242.1:n.2634+208_2634+209delinsAG