Canonical Allele Identifier: CA360268348

Gene: MSH3

Linked Data

• ClinVar Variation Id: 2864132
• ClinVar RCV Id: RCV003702614
• MyVariant Identifiers: chr5:g.79970927A>C (hg19) ; chr5:g.80675108A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675108A>C , CM000667.2:g.80675108A>C	GRCh38
NC_000005.9:g.79970927A>C , CM000667.1:g.79970927A>C	GRCh37
NC_000005.8:g.80006683A>C	NCBI36
NG_016607.1:g.25634A>C
NG_016607.2:g.25634A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1153A>C MANE Select	ENSP00000265081.6:p.Asn385His
ENST00000658259.1:c.985A>C	ENSP00000499617.1:p.Asn329His
ENST00000667069.1:c.1153A>C	ENSP00000499502.1:p.Asn385His
ENST00000670357.1:c.1153A>C	ENSP00000499791.1:p.Asn385His
ENST00000265081.6:c.1153A>C	ENSP00000265081.6:p.Asn385His
NM_002439.4:c.1153A>C	NP_002430.3:p.Asn385His
NM_002439.5:c.1153A>C MANE Select	NP_002430.3:p.Asn385His