Canonical Allele Identifier: CA1873365578
Gene: ALAD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.113389001C= , CM000671.2:g.113389001C= GRCh38
NC_000009.11:g.116151281C= , CM000671.1:g.116151281C= GRCh37
NC_000009.10:g.115191102C= NCBI36
NG_008716.1:g.17338G=

Transcript Alleles

HGVS Amino-acid change
ENST00000409155.8:c.907G= MANE Select ENSP00000386284.3:p.Ala303=
ENST00000409155.7:c.907G= ENSP00000386284.3:p.Ala303=
ENST00000482847.5:n.1180G=
NM_000031.5:c.907G= NP_000022.3:p.Ala303=
XM_005251799.1:c.994G= XP_005251856.1:p.Ala332=
XM_011518363.1:c.1033G= XP_011516665.1:p.Ala345=
XM_011518364.1:c.934G= XP_011516666.1:p.Ala312=
NM_001003945.2:c.994G= NP_001003945.1:p.Ala332=
NM_001317745.1:c.883G= NP_001304674.1:p.Ala295=
XM_011518364.2:c.934G= XP_011516666.1:p.Ala312=
XM_024447449.1:c.994G= XP_024303217.1:p.Ala332=
NM_000031.6:c.907G= MANE Select NP_000022.3:p.Ala303=
NM_001003945.3:c.994G= NP_001003945.1:p.Ala332=
NM_001317745.2:c.883G= NP_001304674.1:p.Ala295=