Canonical Allele Identifier: CA1922577859
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280203G= , CM000672.2:g.80280203G= GRCh38
NC_000010.10:g.82039959G= , CM000672.1:g.82039959G= GRCh37
NC_000010.9:g.82029939G= NCBI36
NG_008083.1:g.14476C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.519C= MANE Select ENSP00000361287.3:p.Leu173=
ENST00000372213.7:c.519C= ENSP00000361287.3:p.Leu173=
ENST00000455001.1:c.330C= ENSP00000414961.1:p.Leu110=
NM_000429.2:c.519C= NP_000420.1:p.Leu173=
XM_005269842.3:c.519C= XP_005269899.1:p.Leu173=
XM_005269843.3:c.396C= XP_005269900.1:p.Leu132=
NM_000429.3:c.519C= MANE Select NP_000420.1:p.Leu173=