Canonical Allele Identifier: CA2658943986

Gene: MSH2

Linked Data

• gnomAD v4: 2-47403090-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403092del , CM000664.2:g.47403092del	GRCh38
NC_000002.11:g.47630231del , CM000664.1:g.47630231del	GRCh37
NC_000002.10:g.47483735del	NCBI36
NG_007110.2:g.4969del , LRG_218:g.4969del

Transcript Alleles

HGVS	Amino-acid change
ENST00000543555.6:c.-114del	ENSP00000442697.1:n.-114del
ENST00000233146.6:c.-100del	ENSP00000233146.2:n.-100del
ENST00000454849.5:c.-114del	ENSP00000411482.1:n.-114del
ENST00000543555.5:c.-114del	ENSP00000442697.1:n.-114del
NM_000251.2:c.-100del , LRG_218t1:c.-100del	NP_000242.1:n.-100del
NM_001258281.1:c.-114del	NP_001245210.1:n.-114del