Canonical Allele Identifier: CA1922573687
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275284C= , CM000672.2:g.80275284C= GRCh38
NC_000010.10:g.82035040C= , CM000672.1:g.82035040C= GRCh37
NC_000010.9:g.82025020C= NCBI36
NG_008083.1:g.19395G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.769-85G= MANE Select ENSP00000361287.3:n.769-85G=
ENST00000372213.7:c.769-85G= ENSP00000361287.3:n.769-85G=
ENST00000485270.5:n.196G=
NM_000429.2:c.769-85G= NP_000420.1:n.769-85G=
XM_005269842.3:c.769-85G= XP_005269899.1:n.769-85G=
XM_005269843.3:c.646-85G= XP_005269900.1:n.646-85G=
NM_000429.3:c.769-85G= MANE Select NP_000420.1:n.769-85G=