Canonical Allele Identifier: CA1873369198
Community Standard Title: NM_000031.6(ALAD):c.-75-3509G=
Gene: ALAD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.113397143C= , CM000671.2:g.113397143C= GRCh38
NC_000009.11:g.116159423C= , CM000671.1:g.116159423C= GRCh37
NC_000009.10:g.115199244C= NCBI36
NG_008716.1:g.9196G=

Transcript Alleles

HGVS Amino-acid Change
NM_000031.6:c.-75-3509G= MANE Select NP_000022.3:n.-75-3509G=
ENST00000409155.8:c.-75-3509G= MANE Select ENSP00000386284.3:n.-75-3509G=
NM_000031.5:c.-75-3509G= NP_000022.3:n.-75-3509G=
NM_001003945.2:c.-154-3509G= NP_001003945.1:n.-154-3509G=
NM_001003945.3:c.-154-3509G= NP_001003945.1:n.-154-3509G=
NM_001317745.1:c.-48-3509G= NP_001304674.1:n.-48-3509G=
NM_001317745.2:c.-48-3509G= NP_001304674.1:n.-48-3509G=
ENST00000409155.7:c.-75-3509G= ENSP00000386284.3:n.-75-3509G=
ENST00000448137.5:c.-49+935G= ENSP00000392748.1:n.-49+935G=
ENST00000452726.1:c.-146G= ENSP00000415737.1:n.-146G=
ENST00000464749.5:n.74-3513G=
ENST00000468504.5:n.48-3509G=
ENST00000482847.5:n.33-3509G=
ENST00000494848.1:n.74-3509G=
XM_005251799.1:c.-154-3509G= XP_005251856.1:n.-154-3509G=
XM_011518363.1:c.-37+935G= XP_011516665.1:n.-37+935G=
XM_011518364.1:c.-146G= XP_011516666.1:n.-146G=
XM_011518364.2:c.-146G= XP_011516666.1:n.-146G=
XM_024447449.1:c.-252G= XP_024303217.1:n.-252G=