Canonical Allele Identifier: CA1873366854

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391846_113391847delinsGA , CM000671.2:g.113391846_113391847delinsGA	GRCh38
NC_000009.11:g.116154126_116154127delinsGA , CM000671.1:g.116154126_116154127delinsGA	GRCh37
NC_000009.10:g.115193947_115193948delinsGA	NCBI36
NG_008716.1:g.14492_14493delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.165-224_165-223delinsTC MANE Select	ENSP00000386284.3:n.165-224_165-223delinsTC
ENST00000409155.7:c.165-224_165-223delinsTC	ENSP00000386284.3:n.165-224_165-223delinsTC
ENST00000448137.5:c.192-224_192-223delinsTC	ENSP00000392748.1:n.192-224_192-223delinsTC
ENST00000464749.5:n.258-914_258-913delinsTC
ENST00000468504.5:n.287-224_287-223delinsTC
ENST00000482001.1:n.438-224_438-223delinsTC
ENST00000482847.5:n.438-224_438-223delinsTC
NM_000031.5:c.165-224_165-223delinsTC	NP_000022.3:n.165-224_165-223delinsTC
XM_005251799.1:c.252-224_252-223delinsTC	XP_005251856.1:n.252-224_252-223delinsTC
XM_011518363.1:c.291-224_291-223delinsTC	XP_011516665.1:n.291-224_291-223delinsTC
XM_011518364.1:c.192-224_192-223delinsTC	XP_011516666.1:n.192-224_192-223delinsTC
NM_001003945.2:c.252-224_252-223delinsTC	NP_001003945.1:n.252-224_252-223delinsTC
NM_001317745.1:c.141-224_141-223delinsTC	NP_001304674.1:n.141-224_141-223delinsTC
XM_011518364.2:c.192-224_192-223delinsTC	XP_011516666.1:n.192-224_192-223delinsTC
XM_024447449.1:c.252-224_252-223delinsTC	XP_024303217.1:n.252-224_252-223delinsTC
XR_002956764.1:n.665-224_665-223delinsTC
NM_000031.6:c.165-224_165-223delinsTC MANE Select	NP_000022.3:n.165-224_165-223delinsTC
NM_001003945.3:c.252-224_252-223delinsTC	NP_001003945.1:n.252-224_252-223delinsTC
NM_001317745.2:c.141-224_141-223delinsTC	NP_001304674.1:n.141-224_141-223delinsTC