Canonical Allele Identifier: CA2691296039

Gene: ALAD

Linked Data

• gnomAD v4: 9-113388837-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113388839dup , CM000671.2:g.113388839dup	GRCh38
NC_000009.11:g.116151119dup , CM000671.1:g.116151119dup	GRCh37
NC_000009.10:g.115190940dup	NCBI36
NG_008716.1:g.17501dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.931+139dup MANE Select	ENSP00000386284.3:n.931+139dup
ENST00000409155.7:c.931+139dup	ENSP00000386284.3:n.931+139dup
ENST00000482847.5:n.1204+139dup
NM_000031.5:c.931+139dup	NP_000022.3:n.931+139dup
XM_005251799.1:c.1018+139dup	XP_005251856.1:n.1018+139dup
XM_011518363.1:c.1057+139dup	XP_011516665.1:n.1057+139dup
XM_011518364.1:c.958+139dup	XP_011516666.1:n.958+139dup
NM_001003945.2:c.1018+139dup	NP_001003945.1:n.1018+139dup
NM_001317745.1:c.907+139dup	NP_001304674.1:n.907+139dup
XM_011518364.2:c.958+139dup	XP_011516666.1:n.958+139dup
XM_024447449.1:c.1018+139dup	XP_024303217.1:n.1018+139dup
NM_000031.6:c.931+139dup MANE Select	NP_000022.3:n.931+139dup
NM_001003945.3:c.1018+139dup	NP_001003945.1:n.1018+139dup
NM_001317745.2:c.907+139dup	NP_001304674.1:n.907+139dup