Canonical Allele Identifier: CA470467323
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82034803T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275047T>C , CM000672.2:g.80275047T>C GRCh38
NC_000010.10:g.82034803T>C , CM000672.1:g.82034803T>C GRCh37
NC_000010.9:g.82024783T>C NCBI36
NG_008083.1:g.19632A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.921A>G MANE Select ENSP00000361287.3:p.Lys307=
ENST00000372213.7:c.921A>G ENSP00000361287.3:p.Lys307=
ENST00000480845.1:n.153A>G
ENST00000485270.5:n.433A>G
NM_000429.2:c.921A>G NP_000420.1:p.Lys307=
XM_005269842.3:c.921A>G XP_005269899.1:p.Lys307=
XM_005269843.3:c.798A>G XP_005269900.1:p.Lys266=
NM_000429.3:c.921A>G MANE Select NP_000420.1:p.Lys307=
Search 100 bp 5'
Search 100 bp 3'