Canonical Allele Identifier: CA1558493956

Gene: MSH3

Linked Data

• dbSNP Id: rs1749814235

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675214del , CM000667.2:g.80675214del	GRCh38
NC_000005.9:g.79971033del , CM000667.1:g.79971033del	GRCh37
NC_000005.8:g.80006789del	NCBI36
NG_016607.1:g.25740del
NG_016607.2:g.25740del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1173+86del MANE Select	ENSP00000265081.6:n.1173+86del
ENST00000658259.1:c.1005+86del	ENSP00000499617.1:n.1005+86del
ENST00000667069.1:c.1173+86del	ENSP00000499502.1:n.1173+86del
ENST00000670357.1:c.1173+86del	ENSP00000499791.1:n.1173+86del
ENST00000265081.6:c.1173+86del	ENSP00000265081.6:n.1173+86del
NM_002439.4:c.1173+86del	NP_002430.3:n.1173+86del
NM_002439.5:c.1173+86del MANE Select	NP_002430.3:n.1173+86del