Canonical Allele Identifier: CA2565914814
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275188_80275189insGG , CM000672.2:g.80275188_80275189insGG GRCh38
NC_000010.10:g.82034944_82034945insGG , CM000672.1:g.82034944_82034945insGG GRCh37
NC_000010.9:g.82024924_82024925insGG NCBI36
NG_008083.1:g.19490_19491insCC

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.779_780insCC MANE Select ENSP00000361287.3:p.Val261LeufsTer?
ENST00000372213.7:c.779_780insCC ENSP00000361287.3:p.Val261LeufsTer?
ENST00000480845.1:n.11_12insCC
ENST00000485270.5:n.291_292insCC
NM_000429.2:c.779_780insCC NP_000420.1:p.Val261LeufsTer?
XM_005269842.3:c.779_780insCC XP_005269899.1:p.Val261LeufsTer?
XM_005269843.3:c.656_657insCC XP_005269900.1:p.Val220LeufsTer?
NM_000429.3:c.779_780insCC MANE Select NP_000420.1:p.Val261LeufsTer?