Canonical Allele Identifier: CA2658944014

Gene: MSH2

Linked Data

• gnomAD v4: 2-47403094-CG-C

Genomic Alleles

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

Transcript Alleles

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