Canonical Allele Identifier: CA1922577842
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80274526A= , CM000672.2:g.80274526A= GRCh38
NC_000010.10:g.82034282A= , CM000672.1:g.82034282A= GRCh37
NC_000010.9:g.82024262A= NCBI36
NG_008083.1:g.20153T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1079T= MANE Select ENSP00000361287.3:p.Ile360=
ENST00000372213.7:c.1079T= ENSP00000361287.3:p.Ile360=
ENST00000480845.1:n.311T=
ENST00000485270.5:n.591T=
NM_000429.2:c.1079T= NP_000420.1:p.Ile360=
XM_005269842.3:c.1079T= XP_005269899.1:p.Ile360=
XM_005269843.3:c.956T= XP_005269900.1:p.Ile319=
NM_000429.3:c.1079T= MANE Select NP_000420.1:p.Ile360=