Canonical Allele Identifier: CA2495876237

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47480971_47480973delinsGTT , CM000664.2:g.47480971_47480973delinsGTT	GRCh38
NC_000002.11:g.47708110_47708112delinsGTT , CM000664.1:g.47708110_47708112delinsGTT	GRCh37
NC_000002.10:g.47561614_47561616delinsGTT	NCBI36
NG_007110.2:g.82848_82850delinsGTT , LRG_218:g.82848_82850delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634+100_2634+102delinsGTT	ENSP00000495641.2:n.2634+100_2634+102delinsGTT
ENST00000233146.7:c.2634+100_2634+102delinsGTT MANE Select	ENSP00000233146.2:n.2634+100_2634+102delinsGTT
ENST00000543555.6:c.2436+100_2436+102delinsGTT	ENSP00000442697.1:n.2436+100_2436+102delinsGTT
ENST00000644092.1:c.*934+100_*934+102delinsGTT	ENSP00000496351.1:n.*934+100_*934+102delinsGTT
ENST00000644900.1:c.487+100_487+102delinsGTT
ENST00000645339.1:c.2634+100_2634+102delinsGTT	ENSP00000496441.1:n.2634+100_2634+102delinsGTT
ENST00000645506.1:c.2634+100_2634+102delinsGTT	ENSP00000495455.1:n.2634+100_2634+102delinsGTT
ENST00000646415.1:c.2634+100_2634+102delinsGTT	ENSP00000495543.1:n.2634+100_2634+102delinsGTT
ENST00000233146.6:c.2634+100_2634+102delinsGTT	ENSP00000233146.2:n.2634+100_2634+102delinsGTT
ENST00000406134.5:c.2634+100_2634+102delinsGTT	ENSP00000384199.1:n.2634+100_2634+102delinsGTT
ENST00000461394.5:n.75+100_75+102delinsGTT
ENST00000543555.5:c.2436+100_2436+102delinsGTT	ENSP00000442697.1:n.2436+100_2436+102delinsGTT
ENST00000610696.4:c.*1030+100_*1030+102delinsGTT	ENSP00000483159.1:n.*1030+100_*1030+102delinsGTT
ENST00000613514.4:c.*1174+100_*1174+102delinsGTT	ENSP00000484137.1:n.*1174+100_*1174+102delinsGTT
ENST00000617333.3:c.*1400+100_*1400+102delinsGTT	ENSP00000482468.1:n.*1400+100_*1400+102delinsGTT
ENST00000617938.4:c.*1606+100_*1606+102delinsGTT	ENSP00000481158.1:n.*1606+100_*1606+102delinsGTT
ENST00000621359.2:c.*200+100_*200+102delinsGTT	ENSP00000481416.1:n.*200+100_*200+102delinsGTT
NM_000251.2:c.2634+100_2634+102delinsGTT , LRG_218t1:c.2634+100_2634+102delinsGTT	NP_000242.1:n.2634+100_2634+102delinsGTT
NM_001258281.1:c.2436+100_2436+102delinsGTT	NP_001245210.1:n.2436+100_2436+102delinsGTT
XM_005264332.2:c.2634+100_2634+102delinsGTT	XP_005264389.2:n.2634+100_2634+102delinsGTT
XM_011532867.1:c.2634+100_2634+102delinsGTT	XP_011531169.1:n.2634+100_2634+102delinsGTT
XR_939685.1:n.2706+100_2706+102delinsGTT
XM_005264332.4:c.2634+100_2634+102delinsGTT	XP_005264389.2:n.2634+100_2634+102delinsGTT
XM_011532867.2:c.2634+100_2634+102delinsGTT	XP_011531169.1:n.2634+100_2634+102delinsGTT
XR_001738747.2:n.2696+100_2696+102delinsGTT
XR_939685.2:n.2696+100_2696+102delinsGTT
NM_000251.3:c.2634+100_2634+102delinsGTT MANE Select	NP_000242.1:n.2634+100_2634+102delinsGTT