Canonical Allele Identifier: CA1922577893
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280234C= , CM000672.2:g.80280234C= GRCh38
NC_000010.10:g.82039990C= , CM000672.1:g.82039990C= GRCh37
NC_000010.9:g.82029970C= NCBI36
NG_008083.1:g.14445G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.488G= MANE Select ENSP00000361287.3:p.Arg163=
ENST00000372213.7:c.488G= ENSP00000361287.3:p.Arg163=
ENST00000455001.1:c.299G= ENSP00000414961.1:p.Arg100=
NM_000429.2:c.488G= NP_000420.1:p.Arg163=
XM_005269842.3:c.488G= XP_005269899.1:p.Arg163=
XM_005269843.3:c.365G= XP_005269900.1:p.Arg122=
NM_000429.3:c.488G= MANE Select NP_000420.1:p.Arg163=