Canonical Allele Identifier: CA2495876333

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47481143_47481146delinsGTTA , CM000664.2:g.47481143_47481146delinsGTTA	GRCh38
NC_000002.11:g.47708282_47708285delinsGTTA , CM000664.1:g.47708282_47708285delinsGTTA	GRCh37
NC_000002.10:g.47561786_47561789delinsGTTA	NCBI36
NG_007110.2:g.83020_83023delinsGTTA , LRG_218:g.83020_83023delinsGTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2634+272_2634+275delinsGTTA	ENSP00000495641.2:n.2634+272_2634+275delinsGTTA
ENST00000233146.7:c.2634+272_2634+275delinsGTTA MANE Select	ENSP00000233146.2:n.2634+272_2634+275delinsGTTA
ENST00000543555.6:c.2436+272_2436+275delinsGTTA	ENSP00000442697.1:n.2436+272_2436+275delinsGTTA
ENST00000644092.1:c.*934+272_*934+275delinsGTTA	ENSP00000496351.1:n.*934+272_*934+275delinsGTTA
ENST00000644900.1:c.487+272_487+275delinsGTTA
ENST00000645339.1:c.2634+272_2634+275delinsGTTA	ENSP00000496441.1:n.2634+272_2634+275delinsGTTA
ENST00000645506.1:c.2634+272_2634+275delinsGTTA	ENSP00000495455.1:n.2634+272_2634+275delinsGTTA
ENST00000646415.1:c.2634+272_2634+275delinsGTTA	ENSP00000495543.1:n.2634+272_2634+275delinsGTTA
ENST00000233146.6:c.2634+272_2634+275delinsGTTA	ENSP00000233146.2:n.2634+272_2634+275delinsGTTA
ENST00000406134.5:c.2634+272_2634+275delinsGTTA	ENSP00000384199.1:n.2634+272_2634+275delinsGTTA
ENST00000461394.5:n.75+272_75+275delinsGTTA
ENST00000543555.5:c.2436+272_2436+275delinsGTTA	ENSP00000442697.1:n.2436+272_2436+275delinsGTTA
ENST00000610696.4:c.*1030+272_*1030+275delinsGTTA	ENSP00000483159.1:n.*1030+272_*1030+275delinsGTTA
ENST00000613514.4:c.*1174+272_*1174+275delinsGTTA	ENSP00000484137.1:n.*1174+272_*1174+275delinsGTTA
ENST00000617333.3:c.*1400+272_*1400+275delinsGTTA	ENSP00000482468.1:n.*1400+272_*1400+275delinsGTTA
ENST00000617938.4:c.*1606+272_*1606+275delinsGTTA	ENSP00000481158.1:n.*1606+272_*1606+275delinsGTTA
ENST00000621359.2:c.*200+272_*200+275delinsGTTA	ENSP00000481416.1:n.*200+272_*200+275delinsGTTA
NM_000251.2:c.2634+272_2634+275delinsGTTA , LRG_218t1:c.2634+272_2634+275delinsGTTA	NP_000242.1:n.2634+272_2634+275delinsGTTA
NM_001258281.1:c.2436+272_2436+275delinsGTTA	NP_001245210.1:n.2436+272_2436+275delinsGTTA
XM_005264332.2:c.2634+272_2634+275delinsGTTA	XP_005264389.2:n.2634+272_2634+275delinsGTTA
XM_011532867.1:c.2634+272_2634+275delinsGTTA	XP_011531169.1:n.2634+272_2634+275delinsGTTA
XR_939685.1:n.2706+272_2706+275delinsGTTA
XM_005264332.4:c.2634+272_2634+275delinsGTTA	XP_005264389.2:n.2634+272_2634+275delinsGTTA
XM_011532867.2:c.2634+272_2634+275delinsGTTA	XP_011531169.1:n.2634+272_2634+275delinsGTTA
XR_001738747.2:n.2696+272_2696+275delinsGTTA
XR_939685.2:n.2696+272_2696+275delinsGTTA
NM_000251.3:c.2634+272_2634+275delinsGTTA MANE Select	NP_000242.1:n.2634+272_2634+275delinsGTTA