Canonical Allele Identifier: CA2609913047
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275270T>G , CM000672.2:g.80275270T>G GRCh38
NC_000010.10:g.82035026T>G , CM000672.1:g.82035026T>G GRCh37
NC_000010.9:g.82025006T>G NCBI36
NG_008083.1:g.19409A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.769-71A>C MANE Select ENSP00000361287.3:n.769-71A>C
ENST00000372213.7:c.769-71A>C ENSP00000361287.3:n.769-71A>C
ENST00000485270.5:n.210A>C
NM_000429.2:c.769-71A>C NP_000420.1:n.769-71A>C
XM_005269842.3:c.769-71A>C XP_005269899.1:n.769-71A>C
XM_005269843.3:c.646-71A>C XP_005269900.1:n.646-71A>C
NM_000429.3:c.769-71A>C MANE Select NP_000420.1:n.769-71A>C