Canonical Allele Identifier: CA1873366783

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391648_113391652delinsTGAAG , CM000671.2:g.113391648_113391652delinsTGAAG	GRCh38
NC_000009.11:g.116153928_116153932delinsTGAAG , CM000671.1:g.116153928_116153932delinsTGAAG	GRCh37
NC_000009.10:g.115193749_115193753delinsTGAAG	NCBI36
NG_008716.1:g.14687_14691delinsCTTCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.165-29_165-25delinsCTTCA MANE Select	ENSP00000386284.3:n.165-29_165-25delinsCT...
ENST00000409155.7:c.165-29_165-25delinsCTTCA	ENSP00000386284.3:n.165-29_165-25delinsCT...
ENST00000448137.5:c.192-29_192-25delinsCTTCA	ENSP00000392748.1:n.192-29_192-25delinsCT...
ENST00000464749.5:n.258-719_258-715delinsCTTCA
ENST00000468504.5:n.287-29_287-25delinsCTTCA
ENST00000482001.1:n.438-29_438-25delinsCTTCA
ENST00000482847.5:n.438-29_438-25delinsCTTCA
NM_000031.5:c.165-29_165-25delinsCTTCA	NP_000022.3:n.165-29_165-25delinsCTTCA
XM_005251799.1:c.252-29_252-25delinsCTTCA	XP_005251856.1:n.252-29_252-25delinsCTTCA...
XM_011518363.1:c.291-29_291-25delinsCTTCA	XP_011516665.1:n.291-29_291-25delinsCTTCA...
XM_011518364.1:c.192-29_192-25delinsCTTCA	XP_011516666.1:n.192-29_192-25delinsCTTCA...
NM_001003945.2:c.252-29_252-25delinsCTTCA	NP_001003945.1:n.252-29_252-25delinsCTTCA...
NM_001317745.1:c.141-29_141-25delinsCTTCA	NP_001304674.1:n.141-29_141-25delinsCTTCA...
XM_011518364.2:c.192-29_192-25delinsCTTCA	XP_011516666.1:n.192-29_192-25delinsCTTCA...
XM_024447449.1:c.252-29_252-25delinsCTTCA	XP_024303217.1:n.252-29_252-25delinsCTTCA...
XR_002956764.1:n.665-29_665-25delinsCTTCA
NM_000031.6:c.165-29_165-25delinsCTTCA MANE Select	NP_000022.3:n.165-29_165-25delinsCTTCA
NM_001003945.3:c.252-29_252-25delinsCTTCA	NP_001003945.1:n.252-29_252-25delinsCTTCA...
NM_001317745.2:c.141-29_141-25delinsCTTCA	NP_001304674.1:n.141-29_141-25delinsCTTCA...