Canonical Allele Identifier: CA445159609

Gene: MSH3

Linked Data

• MyVariant Identifiers: chr5:g.79970812C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80674993C>G , CM000667.2:g.80674993C>G	GRCh38
NC_000005.9:g.79970812C>G , CM000667.1:g.79970812C>G	GRCh37
NC_000005.8:g.80006568C>G	NCBI36
NG_016607.1:g.25519C>G
NG_016607.2:g.25519C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1038C>G MANE Select	ENSP00000265081.6:p.Pro346=
ENST00000658259.1:c.870C>G	ENSP00000499617.1:p.Pro290=
ENST00000667069.1:c.1038C>G	ENSP00000499502.1:p.Pro346=
ENST00000670357.1:c.1038C>G	ENSP00000499791.1:p.Pro346=
ENST00000265081.6:c.1038C>G	ENSP00000265081.6:p.Pro346=
NM_002439.4:c.1038C>G	NP_002430.3:p.Pro346=
NM_002439.5:c.1038C>G MANE Select	NP_002430.3:p.Pro346=