Canonical Allele Identifier: CA2674442881

Gene: MSH3

Linked Data

• gnomAD v4: 5-80674849-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80674849G>T , CM000667.2:g.80674849G>T	GRCh38
NC_000005.9:g.79970668G>T , CM000667.1:g.79970668G>T	GRCh37
NC_000005.8:g.80006424G>T	NCBI36
NG_016607.1:g.25375G>T
NG_016607.2:g.25375G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1028-134G>T MANE Select	ENSP00000265081.6:n.1028-134G>T
ENST00000658259.1:c.860-134G>T	ENSP00000499617.1:n.860-134G>T
ENST00000667069.1:c.1028-134G>T	ENSP00000499502.1:n.1028-134G>T
ENST00000670357.1:c.1028-134G>T	ENSP00000499791.1:n.1028-134G>T
ENST00000265081.6:c.1028-134G>T	ENSP00000265081.6:n.1028-134G>T
NM_002439.4:c.1028-134G>T	NP_002430.3:n.1028-134G>T
NM_002439.5:c.1028-134G>T MANE Select	NP_002430.3:n.1028-134G>T