Canonical Allele Identifier: CA1873365573
Gene: ALAD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.113388994G= , CM000671.2:g.113388994G= GRCh38
NC_000009.11:g.116151274G= , CM000671.1:g.116151274G= GRCh37
NC_000009.10:g.115191095G= NCBI36
NG_008716.1:g.17345C=

Transcript Alleles

HGVS Amino-acid change
ENST00000409155.8:c.914C= MANE Select ENSP00000386284.3:p.Thr305=
ENST00000409155.7:c.914C= ENSP00000386284.3:p.Thr305=
ENST00000482847.5:n.1187C=
NM_000031.5:c.914C= NP_000022.3:p.Thr305=
XM_005251799.1:c.1001C= XP_005251856.1:p.Thr334=
XM_011518363.1:c.1040C= XP_011516665.1:p.Thr347=
XM_011518364.1:c.941C= XP_011516666.1:p.Thr314=
NM_001003945.2:c.1001C= NP_001003945.1:p.Thr334=
NM_001317745.1:c.890C= NP_001304674.1:p.Thr297=
XM_011518364.2:c.941C= XP_011516666.1:p.Thr314=
XM_024447449.1:c.1001C= XP_024303217.1:p.Thr334=
NM_000031.6:c.914C= MANE Select NP_000022.3:p.Thr305=
NM_001003945.3:c.1001C= NP_001003945.1:p.Thr334=
NM_001317745.2:c.890C= NP_001304674.1:p.Thr297=