Canonical Allele Identifier: CA2691297191

Gene: ALAD

Linked Data

• gnomAD v4: 9-113391669-C-CAACG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391670_113391673dup , CM000671.2:g.113391670_113391673dup	GRCh38
NC_000009.11:g.116153950_116153953dup , CM000671.1:g.116153950_116153953dup	GRCh37
NC_000009.10:g.115193771_115193774dup	NCBI36
NG_008716.1:g.14666_14669dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.165-50_165-47dup MANE Select	ENSP00000386284.3:n.165-50_165-47dup
ENST00000409155.7:c.165-50_165-47dup	ENSP00000386284.3:n.165-50_165-47dup
ENST00000448137.5:c.192-50_192-47dup	ENSP00000392748.1:n.192-50_192-47dup
ENST00000464749.5:n.258-740_258-737dup
ENST00000468504.5:n.287-50_287-47dup
ENST00000482001.1:n.438-50_438-47dup
ENST00000482847.5:n.438-50_438-47dup
NM_000031.5:c.165-50_165-47dup	NP_000022.3:n.165-50_165-47dup
XM_005251799.1:c.252-50_252-47dup	XP_005251856.1:n.252-50_252-47dup
XM_011518363.1:c.291-50_291-47dup	XP_011516665.1:n.291-50_291-47dup
XM_011518364.1:c.192-50_192-47dup	XP_011516666.1:n.192-50_192-47dup
NM_001003945.2:c.252-50_252-47dup	NP_001003945.1:n.252-50_252-47dup
NM_001317745.1:c.141-50_141-47dup	NP_001304674.1:n.141-50_141-47dup
XM_011518364.2:c.192-50_192-47dup	XP_011516666.1:n.192-50_192-47dup
XM_024447449.1:c.252-50_252-47dup	XP_024303217.1:n.252-50_252-47dup
XR_002956764.1:n.665-50_665-47dup
NM_000031.6:c.165-50_165-47dup MANE Select	NP_000022.3:n.165-50_165-47dup
NM_001003945.3:c.252-50_252-47dup	NP_001003945.1:n.252-50_252-47dup
NM_001317745.2:c.141-50_141-47dup	NP_001304674.1:n.141-50_141-47dup