Canonical Allele Identifier: CA1922577937
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280310T= , CM000672.2:g.80280310T= GRCh38
NC_000010.10:g.82040066T= , CM000672.1:g.82040066T= GRCh37
NC_000010.9:g.82030046T= NCBI36
NG_008083.1:g.14369A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.412A= MANE Select ENSP00000361287.3:p.Met138=
ENST00000372213.7:c.412A= ENSP00000361287.3:p.Met138=
ENST00000455001.1:c.223A= ENSP00000414961.1:p.Met75=
NM_000429.2:c.412A= NP_000420.1:p.Met138=
XM_005269842.3:c.412A= XP_005269899.1:p.Met138=
XM_005269843.3:c.289A= XP_005269900.1:p.Met97=
NM_000429.3:c.412A= MANE Select NP_000420.1:p.Met138=