Canonical Allele Identifier: CA1922577851
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80274535G= , CM000672.2:g.80274535G= GRCh38
NC_000010.10:g.82034291G= , CM000672.1:g.82034291G= GRCh37
NC_000010.9:g.82024271G= NCBI36
NG_008083.1:g.20144C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1070C= MANE Select ENSP00000361287.3:p.Pro357=
ENST00000372213.7:c.1070C= ENSP00000361287.3:p.Pro357=
ENST00000480845.1:n.302C=
ENST00000485270.5:n.582C=
NM_000429.2:c.1070C= NP_000420.1:p.Pro357=
XM_005269842.3:c.1070C= XP_005269899.1:p.Pro357=
XM_005269843.3:c.947C= XP_005269900.1:p.Pro316=
NM_000429.3:c.1070C= MANE Select NP_000420.1:p.Pro357=