Canonical Allele Identifier: CA360267961
Gene: MSH3 HGNC NCBI

Linked Data

gnomAD v4: 5-80675021-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80675021G>T , CM000667.2:g.80675021G>T GRCh38
NC_000005.9:g.79970840G>T , CM000667.1:g.79970840G>T GRCh37
NC_000005.8:g.80006596G>T NCBI36
NG_016607.1:g.25547G>T
NG_016607.2:g.25547G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.1066G>T MANE Select ENSP00000265081.6:p.Val356Phe
ENST00000658259.1:c.898G>T ENSP00000499617.1:p.Val300Phe
ENST00000667069.1:c.1066G>T ENSP00000499502.1:p.Val356Phe
ENST00000670357.1:c.1066G>T ENSP00000499791.1:p.Val356Phe
ENST00000265081.6:c.1066G>T ENSP00000265081.6:p.Val356Phe
NM_002439.4:c.1066G>T NP_002430.3:p.Val356Phe
NM_002439.5:c.1066G>T MANE Select NP_002430.3:p.Val356Phe