Canonical Allele Identifier: CA2565986298

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113388851_113388854dup , CM000671.2:g.113388851_113388854dup	GRCh38
NC_000009.11:g.116151131_116151134dup , CM000671.1:g.116151131_116151134dup	GRCh37
NC_000009.10:g.115190952_115190955dup	NCBI36
NG_008716.1:g.17488_17491dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.931+126_931+129dup MANE Select	ENSP00000386284.3:n.931+126_931+129dup
ENST00000409155.7:c.931+126_931+129dup	ENSP00000386284.3:n.931+126_931+129dup
ENST00000482847.5:n.1204+126_1204+129dup
NM_000031.5:c.931+126_931+129dup	NP_000022.3:n.931+126_931+129dup
XM_005251799.1:c.1018+126_1018+129dup	XP_005251856.1:n.1018+126_1018+129dup
XM_011518363.1:c.1057+126_1057+129dup	XP_011516665.1:n.1057+126_1057+129dup
XM_011518364.1:c.958+126_958+129dup	XP_011516666.1:n.958+126_958+129dup
NM_001003945.2:c.1018+126_1018+129dup	NP_001003945.1:n.1018+126_1018+129dup
NM_001317745.1:c.907+126_907+129dup	NP_001304674.1:n.907+126_907+129dup
XM_011518364.2:c.958+126_958+129dup	XP_011516666.1:n.958+126_958+129dup
XM_024447449.1:c.1018+126_1018+129dup	XP_024303217.1:n.1018+126_1018+129dup
NM_000031.6:c.931+126_931+129dup MANE Select	NP_000022.3:n.931+126_931+129dup
NM_001003945.3:c.1018+126_1018+129dup	NP_001003945.1:n.1018+126_1018+129dup
NM_001317745.2:c.907+126_907+129dup	NP_001304674.1:n.907+126_907+129dup