Canonical Allele Identifier: CA1873365432

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113388717_113388719delinsCCA , CM000671.2:g.113388717_113388719delinsCCA	GRCh38
NC_000009.11:g.116150997_116150999delinsCCA , CM000671.1:g.116150997_116150999delinsCCA	GRCh37
NC_000009.10:g.115190818_115190820delinsCCA	NCBI36
NG_008716.1:g.17620_17622delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.931+258_931+260delinsTGG MANE Select	ENSP00000386284.3:n.931+258_931+260delinsTGG
ENST00000409155.7:c.931+258_931+260delinsTGG	ENSP00000386284.3:n.931+258_931+260delinsTGG
ENST00000482847.5:n.1204+258_1204+260delinsTGG
NM_000031.5:c.931+258_931+260delinsTGG	NP_000022.3:n.931+258_931+260delinsTGG
XM_005251799.1:c.1018+258_1018+260delinsTGG	XP_005251856.1:n.1018+258_1018+260delinsTGG
XM_011518363.1:c.1057+258_1057+260delinsTGG	XP_011516665.1:n.1057+258_1057+260delinsTGG
XM_011518364.1:c.958+258_958+260delinsTGG	XP_011516666.1:n.958+258_958+260delinsTGG
NM_001003945.2:c.1018+258_1018+260delinsTGG	NP_001003945.1:n.1018+258_1018+260delinsTGG
NM_001317745.1:c.907+258_907+260delinsTGG	NP_001304674.1:n.907+258_907+260delinsTGG
XM_011518364.2:c.958+258_958+260delinsTGG	XP_011516666.1:n.958+258_958+260delinsTGG
XM_024447449.1:c.1018+258_1018+260delinsTGG	XP_024303217.1:n.1018+258_1018+260delinsTGG
NM_000031.6:c.931+258_931+260delinsTGG MANE Select	NP_000022.3:n.931+258_931+260delinsTGG
NM_001003945.3:c.1018+258_1018+260delinsTGG	NP_001003945.1:n.1018+258_1018+260delinsTGG
NM_001317745.2:c.907+258_907+260delinsTGG	NP_001304674.1:n.907+258_907+260delinsTGG