Canonical Allele Identifier: CA470467349
Gene: MAT1A HGNC NCBI

Linked Data

dbSNP Id: rs10887711

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275086A>T , CM000672.2:g.80275086A>T GRCh38
NC_000010.10:g.82034842A>T , CM000672.1:g.82034842A>T GRCh37
NC_000010.9:g.82024822A>T NCBI36
NG_008083.1:g.19593T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.882T>A MANE Select ENSP00000361287.3:p.Ala294=
ENST00000372213.7:c.882T>A ENSP00000361287.3:p.Ala294=
ENST00000480845.1:n.114T>A
ENST00000485270.5:n.394T>A
NM_000429.2:c.882T>A NP_000420.1:p.Ala294=
XM_005269842.3:c.882T>A XP_005269899.1:p.Ala294=
XM_005269843.3:c.759T>A XP_005269900.1:p.Ala253=
NM_000429.3:c.882T>A MANE Select NP_000420.1:p.Ala294=