Canonical Allele Identifier: CA2549650491
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275184_80275185insCAGGCCCGCGTCACCCACGG , CM000672.2:g.80275184_80275185insCAGGCCCGCGTCACCCACGG GRCh38
NC_000010.10:g.82034940_82034941insCAGGCCCGCGTCACCCACGG , CM000672.1:g.82034940_82034941insCAGGCCCGCGTCACCCACGG GRCh37
NC_000010.9:g.82024920_82024921insCAGGCCCGCGTCACCCACGG NCBI36
NG_008083.1:g.19494_19495insCCGTGGGTGACGCGGGCCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.783_784insCCGTGGGTGACGCGGGCCTG MANE Select ENSP00000361287.3:p.Thr262ProfsTer7
ENST00000372213.7:c.783_784insCCGTGGGTGACGCGGGCCTG ENSP00000361287.3:p.Thr262ProfsTer7
ENST00000480845.1:n.15_16insCCGTGGGTGACGCGGGCCTG
ENST00000485270.5:n.295_296insCCGTGGGTGACGCGGGCCTG
NM_000429.2:c.783_784insCCGTGGGTGACGCGGGCCTG NP_000420.1:p.Thr262ProfsTer7
XM_005269842.3:c.783_784insCCGTGGGTGACGCGGGCCTG XP_005269899.1:p.Thr262ProfsTer7
XM_005269843.3:c.660_661insCCGTGGGTGACGCGGGCCTG XP_005269900.1:p.Thr221ProfsTer7
NM_000429.3:c.783_784insCCGTGGGTGACGCGGGCCTG MANE Select NP_000420.1:p.Thr262ProfsTer7