Canonical Allele Identifier: CA2674445893

Gene: MSH3

Linked Data

• gnomAD v4: 5-80873037-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80873037G>T , CM000667.2:g.80873037G>T	GRCh38
NC_000005.9:g.80168856G>T , CM000667.1:g.80168856G>T	GRCh37
NC_000005.8:g.80204612G>T	NCBI36
NG_016607.1:g.223563G>T
NG_016607.2:g.223563G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.3131-79G>T MANE Select	ENSP00000265081.6:n.3131-79G>T
ENST00000658259.1:c.2963-79G>T	ENSP00000499617.1:n.2963-79G>T
ENST00000659302.1:c.539-79G>T
ENST00000667069.1:c.2936-79G>T	ENSP00000499502.1:n.2936-79G>T
ENST00000670357.1:c.*455-79G>T	ENSP00000499791.1:n.*455-79G>T
ENST00000265081.6:c.3131-79G>T	ENSP00000265081.6:n.3131-79G>T
NM_002439.4:c.3131-79G>T	NP_002430.3:n.3131-79G>T
NM_002439.5:c.3131-79G>T MANE Select	NP_002430.3:n.3131-79G>T