Canonical Allele Identifier: CA377360675
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275085C>A , CM000672.2:g.80275085C>A GRCh38
NC_000010.10:g.82034841C>A , CM000672.1:g.82034841C>A GRCh37
NC_000010.9:g.82024821C>A NCBI36
NG_008083.1:g.19594G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.883G>T MANE Select ENSP00000361287.3:p.Ala295Ser
ENST00000372213.7:c.883G>T ENSP00000361287.3:p.Ala295Ser
ENST00000480845.1:n.115G>T
ENST00000485270.5:n.395G>T
NM_000429.2:c.883G>T NP_000420.1:p.Ala295Ser
XM_005269842.3:c.883G>T XP_005269899.1:p.Ala295Ser
XM_005269843.3:c.760G>T XP_005269900.1:p.Ala254Ser
NM_000429.3:c.883G>T MANE Select NP_000420.1:p.Ala295Ser