Canonical Allele Identifier: CA377360782
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275136C>T , CM000672.2:g.80275136C>T GRCh38
NC_000010.10:g.82034892C>T , CM000672.1:g.82034892C>T GRCh37
NC_000010.9:g.82024872C>T NCBI36
NG_008083.1:g.19543G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.832G>A MANE Select ENSP00000361287.3:p.Gly278Ser
ENST00000372213.7:c.832G>A ENSP00000361287.3:p.Gly278Ser
ENST00000480845.1:n.64G>A
ENST00000485270.5:n.344G>A
NM_000429.2:c.832G>A NP_000420.1:p.Gly278Ser
XM_005269842.3:c.832G>A XP_005269899.1:p.Gly278Ser
XM_005269843.3:c.709G>A XP_005269900.1:p.Gly237Ser
NM_000429.3:c.832G>A MANE Select NP_000420.1:p.Gly278Ser