Canonical Allele Identifier: CA2691297166

Gene: ALAD

Linked Data

• gnomAD v4: 9-113391654-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391654A>G , CM000671.2:g.113391654A>G	GRCh38
NC_000009.11:g.116153934A>G , CM000671.1:g.116153934A>G	GRCh37
NC_000009.10:g.115193755A>G	NCBI36
NG_008716.1:g.14685T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.165-31T>C MANE Select	ENSP00000386284.3:n.165-31T>C
ENST00000409155.7:c.165-31T>C	ENSP00000386284.3:n.165-31T>C
ENST00000448137.5:c.192-31T>C	ENSP00000392748.1:n.192-31T>C
ENST00000464749.5:n.258-721T>C
ENST00000468504.5:n.287-31T>C
ENST00000482001.1:n.438-31T>C
ENST00000482847.5:n.438-31T>C
NM_000031.5:c.165-31T>C	NP_000022.3:n.165-31T>C
XM_005251799.1:c.252-31T>C	XP_005251856.1:n.252-31T>C
XM_011518363.1:c.291-31T>C	XP_011516665.1:n.291-31T>C
XM_011518364.1:c.192-31T>C	XP_011516666.1:n.192-31T>C
NM_001003945.2:c.252-31T>C	NP_001003945.1:n.252-31T>C
NM_001317745.1:c.141-31T>C	NP_001304674.1:n.141-31T>C
XM_011518364.2:c.192-31T>C	XP_011516666.1:n.192-31T>C
XM_024447449.1:c.252-31T>C	XP_024303217.1:n.252-31T>C
XR_002956764.1:n.665-31T>C
NM_000031.6:c.165-31T>C MANE Select	NP_000022.3:n.165-31T>C
NM_001003945.3:c.252-31T>C	NP_001003945.1:n.252-31T>C
NM_001317745.2:c.141-31T>C	NP_001304674.1:n.141-31T>C