Canonical Allele Identifier: CA466754907

Gene: ALAD

Linked Data

• gnomAD v4: 9-113389002-C-T
• MyVariant Identifiers: chr9:g.116151282C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389002C>T , CM000671.2:g.113389002C>T	GRCh38
NC_000009.11:g.116151282C>T , CM000671.1:g.116151282C>T	GRCh37
NC_000009.10:g.115191103C>T	NCBI36
NG_008716.1:g.17337G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.906G>A MANE Select	ENSP00000386284.3:p.Glu302=
ENST00000409155.7:c.906G>A	ENSP00000386284.3:p.Glu302=
ENST00000482847.5:n.1179G>A
NM_000031.5:c.906G>A	NP_000022.3:p.Glu302=
XM_005251799.1:c.993G>A	XP_005251856.1:p.Glu331=
XM_011518363.1:c.1032G>A	XP_011516665.1:p.Glu344=
XM_011518364.1:c.933G>A	XP_011516666.1:p.Glu311=
NM_001003945.2:c.993G>A	NP_001003945.1:p.Glu331=
NM_001317745.1:c.882G>A	NP_001304674.1:p.Glu294=
XM_011518364.2:c.933G>A	XP_011516666.1:p.Glu311=
XM_024447449.1:c.993G>A	XP_024303217.1:p.Glu331=
NM_000031.6:c.906G>A MANE Select	NP_000022.3:p.Glu302=
NM_001003945.3:c.993G>A	NP_001003945.1:p.Glu331=
NM_001317745.2:c.882G>A	NP_001304674.1:p.Glu294=