Canonical Allele Identifier: CA377360683
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275090G>C , CM000672.2:g.80275090G>C GRCh38
NC_000010.10:g.82034846G>C , CM000672.1:g.82034846G>C GRCh37
NC_000010.9:g.82024826G>C NCBI36
NG_008083.1:g.19589C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.878C>G MANE Select ENSP00000361287.3:p.Ser293Ter
ENST00000372213.7:c.878C>G ENSP00000361287.3:p.Ser293Ter
ENST00000480845.1:n.110C>G
ENST00000485270.5:n.390C>G
NM_000429.2:c.878C>G NP_000420.1:p.Ser293Ter
XM_005269842.3:c.878C>G XP_005269899.1:p.Ser293Ter
XM_005269843.3:c.755C>G XP_005269900.1:p.Ser252Ter
NM_000429.3:c.878C>G MANE Select NP_000420.1:p.Ser293Ter