Canonical Allele Identifier: CA1922574490
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80276387C= , CM000672.2:g.80276387C= GRCh38
NC_000010.10:g.82036143C= , CM000672.1:g.82036143C= GRCh37
NC_000010.9:g.82026123C= NCBI36
NG_008083.1:g.18292G=

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.757G= MANE Select ENSP00000361287.3:p.Gly253=
ENST00000372213.7:c.757G= ENSP00000361287.3:p.Gly253=
NM_000429.2:c.757G= NP_000420.1:p.Gly253=
XM_005269842.3:c.757G= XP_005269899.1:p.Gly253=
XM_005269843.3:c.634G= XP_005269900.1:p.Gly212=
NM_000429.3:c.757G= MANE Select NP_000420.1:p.Gly253=