Canonical Allele Identifier: CA377360672
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275084G>A , CM000672.2:g.80275084G>A GRCh38
NC_000010.10:g.82034840G>A , CM000672.1:g.82034840G>A GRCh37
NC_000010.9:g.82024820G>A NCBI36
NG_008083.1:g.19595C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.884C>T MANE Select ENSP00000361287.3:p.Ala295Val
ENST00000372213.7:c.884C>T ENSP00000361287.3:p.Ala295Val
ENST00000480845.1:n.116C>T
ENST00000485270.5:n.396C>T
NM_000429.2:c.884C>T NP_000420.1:p.Ala295Val
XM_005269842.3:c.884C>T XP_005269899.1:p.Ala295Val
XM_005269843.3:c.761C>T XP_005269900.1:p.Ala254Val
NM_000429.3:c.884C>T MANE Select NP_000420.1:p.Ala295Val