Canonical Allele Identifier: CA374562928

Gene: ALAD

Linked Data

• gnomAD v4: 9-113388991-G-T
• MyVariant Identifiers: chr9:g.116151271G>T (hg19) ; chr9:g.113388991G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113388991G>T , CM000671.2:g.113388991G>T	GRCh38
NC_000009.11:g.116151271G>T , CM000671.1:g.116151271G>T	GRCh37
NC_000009.10:g.115191092G>T	NCBI36
NG_008716.1:g.17348C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.917C>A MANE Select	ENSP00000386284.3:p.Ala306Asp
ENST00000409155.7:c.917C>A	ENSP00000386284.3:p.Ala306Asp
ENST00000482847.5:n.1190C>A
NM_000031.5:c.917C>A	NP_000022.3:p.Ala306Asp
XM_005251799.1:c.1004C>A	XP_005251856.1:p.Ala335Asp
XM_011518363.1:c.1043C>A	XP_011516665.1:p.Ala348Asp
XM_011518364.1:c.944C>A	XP_011516666.1:p.Ala315Asp
NM_001003945.2:c.1004C>A	NP_001003945.1:p.Ala335Asp
NM_001317745.1:c.893C>A	NP_001304674.1:p.Ala298Asp
XM_011518364.2:c.944C>A	XP_011516666.1:p.Ala315Asp
XM_024447449.1:c.1004C>A	XP_024303217.1:p.Ala335Asp
NM_000031.6:c.917C>A MANE Select	NP_000022.3:p.Ala306Asp
NM_001003945.3:c.1004C>A	NP_001003945.1:p.Ala335Asp
NM_001317745.2:c.893C>A	NP_001304674.1:p.Ala298Asp