Canonical Allele Identifier: CA377362872
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82040062A>C (hg19) chr10:g.80280306A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280306A>C , CM000672.2:g.80280306A>C GRCh38
NC_000010.10:g.82040062A>C , CM000672.1:g.82040062A>C GRCh37
NC_000010.9:g.82030042A>C NCBI36
NG_008083.1:g.14373T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.416T>G MANE Select ENSP00000361287.3:p.Phe139Cys
ENST00000372213.7:c.416T>G ENSP00000361287.3:p.Phe139Cys
ENST00000455001.1:c.227T>G ENSP00000414961.1:p.Phe76Cys
NM_000429.2:c.416T>G NP_000420.1:p.Phe139Cys
XM_005269842.3:c.416T>G XP_005269899.1:p.Phe139Cys
XM_005269843.3:c.293T>G XP_005269900.1:p.Phe98Cys
NM_000429.3:c.416T>G MANE Select NP_000420.1:p.Phe139Cys
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