Canonical Allele Identifier: CA2495826421

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403096_47403097delinsGA , CM000664.2:g.47403096_47403097delinsGA	GRCh38
NC_000002.11:g.47630235_47630236delinsGA , CM000664.1:g.47630235_47630236delinsGA	GRCh37
NC_000002.10:g.47483739_47483740delinsGA	NCBI36
NG_007110.2:g.4973_4974delinsGA , LRG_218:g.4973_4974delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000543555.6:c.-110_-109delinsGA	ENSP00000442697.1:n.-110_-109delinsGA
ENST00000233146.6:c.-96_-95delinsGA	ENSP00000233146.2:n.-96_-95delinsGA
ENST00000454849.5:c.-110_-109delinsGA	ENSP00000411482.1:n.-110_-109delinsGA
ENST00000543555.5:c.-110_-109delinsGA	ENSP00000442697.1:n.-110_-109delinsGA
NM_000251.2:c.-96_-95delinsGA , LRG_218t1:c.-96_-95delinsGA	NP_000242.1:n.-96_-95delinsGA
NM_001258281.1:c.-110_-109delinsGA	NP_001245210.1:n.-110_-109delinsGA