Canonical Allele Identifier: CA1873366851

Gene: ALAD

Linked Data

• dbSNP Id: rs1827594380

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391842del , CM000671.2:g.113391842del	GRCh38
NC_000009.11:g.116154122del , CM000671.1:g.116154122del	GRCh37
NC_000009.10:g.115193943del	NCBI36
NG_008716.1:g.14498del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.165-218del MANE Select	ENSP00000386284.3:n.165-218del
ENST00000409155.7:c.165-218del	ENSP00000386284.3:n.165-218del
ENST00000448137.5:c.192-218del	ENSP00000392748.1:n.192-218del
ENST00000464749.5:n.258-908del
ENST00000468504.5:n.287-218del
ENST00000482001.1:n.438-218del
ENST00000482847.5:n.438-218del
NM_000031.5:c.165-218del	NP_000022.3:n.165-218del
XM_005251799.1:c.252-218del	XP_005251856.1:n.252-218del
XM_011518363.1:c.291-218del	XP_011516665.1:n.291-218del
XM_011518364.1:c.192-218del	XP_011516666.1:n.192-218del
NM_001003945.2:c.252-218del	NP_001003945.1:n.252-218del
NM_001317745.1:c.141-218del	NP_001304674.1:n.141-218del
XM_011518364.2:c.192-218del	XP_011516666.1:n.192-218del
XM_024447449.1:c.252-218del	XP_024303217.1:n.252-218del
XR_002956764.1:n.665-218del
NM_000031.6:c.165-218del MANE Select	NP_000022.3:n.165-218del
NM_001003945.3:c.252-218del	NP_001003945.1:n.252-218del
NM_001317745.2:c.141-218del	NP_001304674.1:n.141-218del