Canonical Allele Identifier: CA377360165
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82033608T>C (hg19) chr10:g.80273852T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273852T>C , CM000672.2:g.80273852T>C GRCh38
NC_000010.10:g.82033608T>C , CM000672.1:g.82033608T>C GRCh37
NC_000010.9:g.82023588T>C NCBI36
NG_008083.1:g.20827A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1117A>G MANE Select ENSP00000361287.3:p.Lys373Glu
ENST00000372213.7:c.1117A>G ENSP00000361287.3:p.Lys373Glu
ENST00000480845.1:n.349A>G
ENST00000485270.5:n.629A>G
NM_000429.2:c.1117A>G NP_000420.1:p.Lys373Glu
XM_005269842.3:c.1117A>G XP_005269899.1:p.Lys373Glu
XM_005269843.3:c.994A>G XP_005269900.1:p.Lys332Glu
NM_000429.3:c.1117A>G MANE Select NP_000420.1:p.Lys373Glu
Search 100 bp 5'
Search 100 bp 3'