Canonical Allele Identifier: CA377360755
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82034879A>T (hg19) chr10:g.80275123A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275123A>T , CM000672.2:g.80275123A>T GRCh38
NC_000010.10:g.82034879A>T , CM000672.1:g.82034879A>T GRCh37
NC_000010.9:g.82024859A>T NCBI36
NG_008083.1:g.19556T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.845T>A MANE Select ENSP00000361287.3:p.Phe282Tyr
ENST00000372213.7:c.845T>A ENSP00000361287.3:p.Phe282Tyr
ENST00000480845.1:n.77T>A
ENST00000485270.5:n.357T>A
NM_000429.2:c.845T>A NP_000420.1:p.Phe282Tyr
XM_005269842.3:c.845T>A XP_005269899.1:p.Phe282Tyr
XM_005269843.3:c.722T>A XP_005269900.1:p.Phe241Tyr
NM_000429.3:c.845T>A MANE Select NP_000420.1:p.Phe282Tyr
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