Canonical Allele Identifier: CA377360955
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275190C>A , CM000672.2:g.80275190C>A GRCh38
NC_000010.10:g.82034946C>A , CM000672.1:g.82034946C>A GRCh37
NC_000010.9:g.82024926C>A NCBI36
NG_008083.1:g.19489G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.778G>T MANE Select ENSP00000361287.3:p.Gly260Cys
ENST00000372213.7:c.778G>T ENSP00000361287.3:p.Gly260Cys
ENST00000480845.1:n.10G>T
ENST00000485270.5:n.290G>T
NM_000429.2:c.778G>T NP_000420.1:p.Gly260Cys
XM_005269842.3:c.778G>T XP_005269899.1:p.Gly260Cys
XM_005269843.3:c.655G>T XP_005269900.1:p.Gly219Cys
NM_000429.3:c.778G>T MANE Select NP_000420.1:p.Gly260Cys