Canonical Allele Identifier: CA2691297327

Gene: ALAD

Linked Data

• gnomAD v4: 9-113391739-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391739G>T , CM000671.2:g.113391739G>T	GRCh38
NC_000009.11:g.116154019G>T , CM000671.1:g.116154019G>T	GRCh37
NC_000009.10:g.115193840G>T	NCBI36
NG_008716.1:g.14600C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.165-116C>A MANE Select	ENSP00000386284.3:n.165-116C>A
ENST00000409155.7:c.165-116C>A	ENSP00000386284.3:n.165-116C>A
ENST00000448137.5:c.192-116C>A	ENSP00000392748.1:n.192-116C>A
ENST00000464749.5:n.258-806C>A
ENST00000468504.5:n.287-116C>A
ENST00000482001.1:n.438-116C>A
ENST00000482847.5:n.438-116C>A
NM_000031.5:c.165-116C>A	NP_000022.3:n.165-116C>A
XM_005251799.1:c.252-116C>A	XP_005251856.1:n.252-116C>A
XM_011518363.1:c.291-116C>A	XP_011516665.1:n.291-116C>A
XM_011518364.1:c.192-116C>A	XP_011516666.1:n.192-116C>A
NM_001003945.2:c.252-116C>A	NP_001003945.1:n.252-116C>A
NM_001317745.1:c.141-116C>A	NP_001304674.1:n.141-116C>A
XM_011518364.2:c.192-116C>A	XP_011516666.1:n.192-116C>A
XM_024447449.1:c.252-116C>A	XP_024303217.1:n.252-116C>A
XR_002956764.1:n.665-116C>A
NM_000031.6:c.165-116C>A MANE Select	NP_000022.3:n.165-116C>A
NM_001003945.3:c.252-116C>A	NP_001003945.1:n.252-116C>A
NM_001317745.2:c.141-116C>A	NP_001304674.1:n.141-116C>A