Canonical Allele Identifier: CA2785629580

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113388981_113389031del , CM000671.2:g.113388981_113389031del	GRCh38
NC_000009.11:g.116151261_116151311del , CM000671.1:g.116151261_116151311del	GRCh37
NC_000009.10:g.115191082_115191132del	NCBI36
NG_008716.1:g.17311_17361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.880_930del MANE Select	ENSP00000386284.3:p.Phe294_Ala310del
ENST00000409155.7:c.880_930del	ENSP00000386284.3:p.Phe294_Ala310del
ENST00000482847.5:n.1153_1203del
NM_000031.5:c.880_930del	NP_000022.3:p.Phe294_Ala310del
XM_005251799.1:c.967_1017del	XP_005251856.1:p.Phe323_Ala339del
XM_011518363.1:c.1006_1056del	XP_011516665.1:p.Phe336_Ala352del
XM_011518364.1:c.907_957del	XP_011516666.1:p.Phe303_Ala319del
NM_001003945.2:c.967_1017del	NP_001003945.1:p.Phe323_Ala339del
NM_001317745.1:c.856_906del	NP_001304674.1:p.Phe286_Ala302del
XM_011518364.2:c.907_957del	XP_011516666.1:p.Phe303_Ala319del
XM_024447449.1:c.967_1017del	XP_024303217.1:p.Phe323_Ala339del
NM_000031.6:c.880_930del MANE Select	NP_000022.3:p.Phe294_Ala310del
NM_001003945.3:c.967_1017del	NP_001003945.1:p.Phe323_Ala339del
NM_001317745.2:c.856_906del	NP_001304674.1:p.Phe286_Ala302del