Canonical Allele Identifier: CA374565118

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116153858T>A (hg19) ; chr9:g.113391578T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391578T>A , CM000671.2:g.113391578T>A	GRCh38
NC_000009.11:g.116153858T>A , CM000671.1:g.116153858T>A	GRCh37
NC_000009.10:g.115193679T>A	NCBI36
NG_008716.1:g.14761A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.210A>T MANE Select	ENSP00000386284.3:p.Glu70Asp
ENST00000409155.7:c.210A>T	ENSP00000386284.3:p.Glu70Asp
ENST00000448137.5:c.237A>T	ENSP00000392748.1:p.Glu79Asp
ENST00000464749.5:n.258-645A>T
ENST00000468504.5:n.332A>T
ENST00000482001.1:n.483A>T
ENST00000482847.5:n.483A>T
NM_000031.5:c.210A>T	NP_000022.3:p.Glu70Asp
XM_005251799.1:c.297A>T	XP_005251856.1:p.Glu99Asp
XM_011518363.1:c.336A>T	XP_011516665.1:p.Glu112Asp
XM_011518364.1:c.237A>T	XP_011516666.1:p.Glu79Asp
NM_001003945.2:c.297A>T	NP_001003945.1:p.Glu99Asp
NM_001317745.1:c.186A>T	NP_001304674.1:p.Glu62Asp
XM_011518364.2:c.237A>T	XP_011516666.1:p.Glu79Asp
XM_024447449.1:c.297A>T	XP_024303217.1:p.Glu99Asp
XR_002956764.1:n.710A>T
NM_000031.6:c.210A>T MANE Select	NP_000022.3:p.Glu70Asp
NM_001003945.3:c.297A>T	NP_001003945.1:p.Glu99Asp
NM_001317745.2:c.186A>T	NP_001304674.1:p.Glu62Asp