Canonical Allele Identifier: CA470467363
Gene: MAT1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.82034866_82034867insGGA (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275110_80275111insGGA , CM000672.2:g.80275110_80275111insGGA GRCh38
NC_000010.10:g.82034866_82034867insGGA , CM000672.1:g.82034866_82034867insGGA GRCh37
NC_000010.9:g.82024846_82024847insGGA NCBI36
NG_008083.1:g.19568_19569insTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.857_858insTCC MANE Select ENSP00000361287.3:p.Asp286_Tyr287insPro
ENST00000372213.7:c.857_858insTCC ENSP00000361287.3:p.Asp286_Tyr287insPro
ENST00000480845.1:n.89_90insTCC
ENST00000485270.5:n.369_370insTCC
NM_000429.2:c.857_858insTCC NP_000420.1:p.Asp286_Tyr287insPro
XM_005269842.3:c.857_858insTCC XP_005269899.1:p.Asp286_Tyr287insPro
XM_005269843.3:c.734_735insTCC XP_005269900.1:p.Asp245_Tyr246insPro
NM_000429.3:c.857_858insTCC MANE Select NP_000420.1:p.Asp286_Tyr287insPro
Search 100 bp 5'
Search 100 bp 3'