Canonical Allele Identifier: CA377360669
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275082A>C , CM000672.2:g.80275082A>C GRCh38
NC_000010.10:g.82034838A>C , CM000672.1:g.82034838A>C GRCh37
NC_000010.9:g.82024818A>C NCBI36
NG_008083.1:g.19597T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.886T>G MANE Select ENSP00000361287.3:p.Tyr296Asp
ENST00000372213.7:c.886T>G ENSP00000361287.3:p.Tyr296Asp
ENST00000480845.1:n.118T>G
ENST00000485270.5:n.398T>G
NM_000429.2:c.886T>G NP_000420.1:p.Tyr296Asp
XM_005269842.3:c.886T>G XP_005269899.1:p.Tyr296Asp
XM_005269843.3:c.763T>G XP_005269900.1:p.Tyr255Asp
NM_000429.3:c.886T>G MANE Select NP_000420.1:p.Tyr296Asp