Canonical Allele Identifier: CA1922573525
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275156T= , CM000672.2:g.80275156T= GRCh38
NC_000010.10:g.82034912T= , CM000672.1:g.82034912T= GRCh37
NC_000010.9:g.82024892T= NCBI36
NG_008083.1:g.19523A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.812A= MANE Select ENSP00000361287.3:p.Tyr271=
ENST00000372213.7:c.812A= ENSP00000361287.3:p.Tyr271=
ENST00000480845.1:n.44A=
ENST00000485270.5:n.324A=
NM_000429.2:c.812A= NP_000420.1:p.Tyr271=
XM_005269842.3:c.812A= XP_005269899.1:p.Tyr271=
XM_005269843.3:c.689A= XP_005269900.1:p.Tyr230=
NM_000429.3:c.812A= MANE Select NP_000420.1:p.Tyr271=