Canonical Allele Identifier: CA377360680
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275088C>G , CM000672.2:g.80275088C>G GRCh38
NC_000010.10:g.82034844C>G , CM000672.1:g.82034844C>G GRCh37
NC_000010.9:g.82024824C>G NCBI36
NG_008083.1:g.19591G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.880G>C MANE Select ENSP00000361287.3:p.Ala294Pro
ENST00000372213.7:c.880G>C ENSP00000361287.3:p.Ala294Pro
ENST00000480845.1:n.112G>C
ENST00000485270.5:n.392G>C
NM_000429.2:c.880G>C NP_000420.1:p.Ala294Pro
XM_005269842.3:c.880G>C XP_005269899.1:p.Ala294Pro
XM_005269843.3:c.757G>C XP_005269900.1:p.Ala253Pro
NM_000429.3:c.880G>C MANE Select NP_000420.1:p.Ala294Pro