Canonical Allele Identifier: CA377362668
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82039969G>T (hg19) chr10:g.80280213G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280213G>T , CM000672.2:g.80280213G>T GRCh38
NC_000010.10:g.82039969G>T , CM000672.1:g.82039969G>T GRCh37
NC_000010.9:g.82029949G>T NCBI36
NG_008083.1:g.14466C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.509C>A MANE Select ENSP00000361287.3:p.Ser170Tyr
ENST00000372213.7:c.509C>A ENSP00000361287.3:p.Ser170Tyr
ENST00000455001.1:c.320C>A ENSP00000414961.1:p.Ser107Tyr
NM_000429.2:c.509C>A NP_000420.1:p.Ser170Tyr
XM_005269842.3:c.509C>A XP_005269899.1:p.Ser170Tyr
XM_005269843.3:c.386C>A XP_005269900.1:p.Ser129Tyr
NM_000429.3:c.509C>A MANE Select NP_000420.1:p.Ser170Tyr
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