Canonical Allele Identifier: CA2579424465

Gene: ALAD

Linked Data

• gnomAD v4: 9-113391643-GGGGTTGAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391646_113391653del , CM000671.2:g.113391646_113391653del	GRCh38
NC_000009.11:g.116153926_116153933del , CM000671.1:g.116153926_116153933del	GRCh37
NC_000009.10:g.115193747_115193754del	NCBI36
NG_008716.1:g.14688_14695del

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.165-28_165-21del MANE Select	ENSP00000386284.3:n.165-28_165-21del
ENST00000409155.7:c.165-28_165-21del	ENSP00000386284.3:n.165-28_165-21del
ENST00000448137.5:c.192-28_192-21del	ENSP00000392748.1:n.192-28_192-21del
ENST00000464749.5:n.258-718_258-711del
ENST00000468504.5:n.287-28_287-21del
ENST00000482001.1:n.438-28_438-21del
ENST00000482847.5:n.438-28_438-21del
NM_000031.5:c.165-28_165-21del	NP_000022.3:n.165-28_165-21del
XM_005251799.1:c.252-28_252-21del	XP_005251856.1:n.252-28_252-21del
XM_011518363.1:c.291-28_291-21del	XP_011516665.1:n.291-28_291-21del
XM_011518364.1:c.192-28_192-21del	XP_011516666.1:n.192-28_192-21del
NM_001003945.2:c.252-28_252-21del	NP_001003945.1:n.252-28_252-21del
NM_001317745.1:c.141-28_141-21del	NP_001304674.1:n.141-28_141-21del
XM_011518364.2:c.192-28_192-21del	XP_011516666.1:n.192-28_192-21del
XM_024447449.1:c.252-28_252-21del	XP_024303217.1:n.252-28_252-21del
XR_002956764.1:n.665-28_665-21del
NM_000031.6:c.165-28_165-21del MANE Select	NP_000022.3:n.165-28_165-21del
NM_001003945.3:c.252-28_252-21del	NP_001003945.1:n.252-28_252-21del
NM_001317745.2:c.141-28_141-21del	NP_001304674.1:n.141-28_141-21del