Canonical Allele Identifier: CA1873366781
Gene: ALAD HGNC NCBI

Linked Data

dbSNP Id: rs759495380

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.113391647T>A , CM000671.2:g.113391647T>A GRCh38
NC_000009.11:g.116153927T>A , CM000671.1:g.116153927T>A GRCh37
NC_000009.10:g.115193748T>A NCBI36
NG_008716.1:g.14692A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000409155.8:c.165-24A>T MANE Select ENSP00000386284.3:n.165-24A>T
ENST00000409155.7:c.165-24A>T ENSP00000386284.3:n.165-24A>T
ENST00000448137.5:c.192-24A>T ENSP00000392748.1:n.192-24A>T
ENST00000464749.5:n.258-714A>T
ENST00000468504.5:n.287-24A>T
ENST00000482001.1:n.438-24A>T
ENST00000482847.5:n.438-24A>T
NM_000031.5:c.165-24A>T NP_000022.3:n.165-24A>T
XM_005251799.1:c.252-24A>T XP_005251856.1:n.252-24A>T
XM_011518363.1:c.291-24A>T XP_011516665.1:n.291-24A>T
XM_011518364.1:c.192-24A>T XP_011516666.1:n.192-24A>T
NM_001003945.2:c.252-24A>T NP_001003945.1:n.252-24A>T
NM_001317745.1:c.141-24A>T NP_001304674.1:n.141-24A>T
XM_011518364.2:c.192-24A>T XP_011516666.1:n.192-24A>T
XM_024447449.1:c.252-24A>T XP_024303217.1:n.252-24A>T
XR_002956764.1:n.665-24A>T
NM_000031.6:c.165-24A>T MANE Select NP_000022.3:n.165-24A>T
NM_001003945.3:c.252-24A>T NP_001003945.1:n.252-24A>T
NM_001317745.2:c.141-24A>T NP_001304674.1:n.141-24A>T