Canonical Allele Identifier: CA360267946

Gene: MSH3

Linked Data

• gnomAD v4: 5-80675019-A-G
• MyVariant Identifiers: chr5:g.79970838A>G (hg19) ; chr5:g.80675019A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675019A>G , CM000667.2:g.80675019A>G	GRCh38
NC_000005.9:g.79970838A>G , CM000667.1:g.79970838A>G	GRCh37
NC_000005.8:g.80006594A>G	NCBI36
NG_016607.1:g.25545A>G
NG_016607.2:g.25545A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1064A>G MANE Select	ENSP00000265081.6:p.Asn355Ser
ENST00000658259.1:c.896A>G	ENSP00000499617.1:p.Asn299Ser
ENST00000667069.1:c.1064A>G	ENSP00000499502.1:p.Asn355Ser
ENST00000670357.1:c.1064A>G	ENSP00000499791.1:p.Asn355Ser
ENST00000265081.6:c.1064A>G	ENSP00000265081.6:p.Asn355Ser
NM_002439.4:c.1064A>G	NP_002430.3:p.Asn355Ser
NM_002439.5:c.1064A>G MANE Select	NP_002430.3:p.Asn355Ser