Canonical Allele Identifier: CA360267986
Gene: MSH3 HGNC NCBI

Linked Data

gnomAD v4: 5-80675027-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80675027G>A , CM000667.2:g.80675027G>A GRCh38
NC_000005.9:g.79970846G>A , CM000667.1:g.79970846G>A GRCh37
NC_000005.8:g.80006602G>A NCBI36
NG_016607.1:g.25553G>A
NG_016607.2:g.25553G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.1072G>A MANE Select ENSP00000265081.6:p.Glu358Lys
ENST00000658259.1:c.904G>A ENSP00000499617.1:p.Glu302Lys
ENST00000667069.1:c.1072G>A ENSP00000499502.1:p.Glu358Lys
ENST00000670357.1:c.1072G>A ENSP00000499791.1:p.Glu358Lys
ENST00000265081.6:c.1072G>A ENSP00000265081.6:p.Glu358Lys
NM_002439.4:c.1072G>A NP_002430.3:p.Glu358Lys
NM_002439.5:c.1072G>A MANE Select NP_002430.3:p.Glu358Lys