Canonical Allele Identifier: CA2674442878

Gene: MSH3

Linked Data

• gnomAD v4: 5-80674839-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80674842del , CM000667.2:g.80674842del	GRCh38
NC_000005.9:g.79970661del , CM000667.1:g.79970661del	GRCh37
NC_000005.8:g.80006417del	NCBI36
NG_016607.1:g.25368del
NG_016607.2:g.25368del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1028-141del MANE Select	ENSP00000265081.6:n.1028-141del
ENST00000658259.1:c.860-141del	ENSP00000499617.1:n.860-141del
ENST00000667069.1:c.1028-141del	ENSP00000499502.1:n.1028-141del
ENST00000670357.1:c.1028-141del	ENSP00000499791.1:n.1028-141del
ENST00000265081.6:c.1028-141del	ENSP00000265081.6:n.1028-141del
NM_002439.4:c.1028-141del	NP_002430.3:n.1028-141del
NM_002439.5:c.1028-141del MANE Select	NP_002430.3:n.1028-141del