Canonical Allele Identifier: CA1922574494
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80276389A= , CM000672.2:g.80276389A= GRCh38
NC_000010.10:g.82036145A= , CM000672.1:g.82036145A= GRCh37
NC_000010.9:g.82026125A= NCBI36
NG_008083.1:g.18290T=

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.755T= MANE Select ENSP00000361287.3:p.Ile252=
ENST00000372213.7:c.755T= ENSP00000361287.3:p.Ile252=
NM_000429.2:c.755T= NP_000420.1:p.Ile252=
XM_005269842.3:c.755T= XP_005269899.1:p.Ile252=
XM_005269843.3:c.632T= XP_005269900.1:p.Ile211=
NM_000429.3:c.755T= MANE Select NP_000420.1:p.Ile252=