Canonical Allele Identifier: CA1922578023
Gene: MAT1A HGNC NCBI

Linked Data

dbSNP Id: rs1043114384

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280466T>A , CM000672.2:g.80280466T>A GRCh38
NC_000010.10:g.82040222T>A , CM000672.1:g.82040222T>A GRCh37
NC_000010.9:g.82030202T>A NCBI36
NG_008083.1:g.14213A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.406-150A>T MANE Select ENSP00000361287.3:n.406-150A>T
ENST00000372213.7:c.406-150A>T ENSP00000361287.3:n.406-150A>T
ENST00000455001.1:c.217-150A>T ENSP00000414961.1:n.217-150A>T
NM_000429.2:c.406-150A>T NP_000420.1:n.406-150A>T
XM_005269842.3:c.406-150A>T XP_005269899.1:n.406-150A>T
XM_005269843.3:c.283-150A>T XP_005269900.1:n.283-150A>T
NM_000429.3:c.406-150A>T MANE Select NP_000420.1:n.406-150A>T