Canonical Allele Identifier: CA1873366776
Gene: ALAD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.113391643G= , CM000671.2:g.113391643G= GRCh38
NC_000009.11:g.116153923G= , CM000671.1:g.116153923G= GRCh37
NC_000009.10:g.115193744G= NCBI36
NG_008716.1:g.14696C=

Transcript Alleles

HGVS Amino-acid change
ENST00000409155.8:c.165-20C= MANE Select ENSP00000386284.3:n.165-20C=
ENST00000409155.7:c.165-20C= ENSP00000386284.3:n.165-20C=
ENST00000448137.5:c.192-20C= ENSP00000392748.1:n.192-20C=
ENST00000464749.5:n.258-710C=
ENST00000468504.5:n.287-20C=
ENST00000482001.1:n.438-20C=
ENST00000482847.5:n.438-20C=
NM_000031.5:c.165-20C= NP_000022.3:n.165-20C=
XM_005251799.1:c.252-20C= XP_005251856.1:n.252-20C=
XM_011518363.1:c.291-20C= XP_011516665.1:n.291-20C=
XM_011518364.1:c.192-20C= XP_011516666.1:n.192-20C=
NM_001003945.2:c.252-20C= NP_001003945.1:n.252-20C=
NM_001317745.1:c.141-20C= NP_001304674.1:n.141-20C=
XM_011518364.2:c.192-20C= XP_011516666.1:n.192-20C=
XM_024447449.1:c.252-20C= XP_024303217.1:n.252-20C=
XR_002956764.1:n.665-20C=
NM_000031.6:c.165-20C= MANE Select NP_000022.3:n.165-20C=
NM_001003945.3:c.252-20C= NP_001003945.1:n.252-20C=
NM_001317745.2:c.141-20C= NP_001304674.1:n.141-20C=