Canonical Allele Identifier: CA1922573860
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275530T= , CM000672.2:g.80275530T= GRCh38
NC_000010.10:g.82035286T= , CM000672.1:g.82035286T= GRCh37
NC_000010.9:g.82025266T= NCBI36
NG_008083.1:g.19149A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.769-331A= MANE Select ENSP00000361287.3:n.769-331A=
ENST00000372213.7:c.769-331A= ENSP00000361287.3:n.769-331A=
NM_000429.2:c.769-331A= NP_000420.1:n.769-331A=
XM_005269842.3:c.769-331A= XP_005269899.1:n.769-331A=
XM_005269843.3:c.646-331A= XP_005269900.1:n.646-331A=
NM_000429.3:c.769-331A= MANE Select NP_000420.1:n.769-331A=