Canonical Allele Identifier: CA1922573363
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275080A= , CM000672.2:g.80275080A= GRCh38
NC_000010.10:g.82034836A= , CM000672.1:g.82034836A= GRCh37
NC_000010.9:g.82024816A= NCBI36
NG_008083.1:g.19599T=

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.888T= MANE Select ENSP00000361287.3:p.Tyr296=
ENST00000372213.7:c.888T= ENSP00000361287.3:p.Tyr296=
ENST00000480845.1:n.120T=
ENST00000485270.5:n.400T=
NM_000429.2:c.888T= NP_000420.1:p.Tyr296=
XM_005269842.3:c.888T= XP_005269899.1:p.Tyr296=
XM_005269843.3:c.765T= XP_005269900.1:p.Tyr255=
NM_000429.3:c.888T= MANE Select NP_000420.1:p.Tyr296=