Canonical Allele Identifier: CA1630847959

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391611C= , CM000671.2:g.113391611C=	GRCh38
NC_000009.11:g.116153891C= , CM000671.1:g.116153891C=	GRCh37
NC_000009.10:g.115193712C=	NCBI36
NG_008716.1:g.14728G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000031.6:c.177G= MANE Select	NP_000022.3:p.Lys59=
ENST00000409155.8:c.177G= MANE Select	ENSP00000386284.3:p.Lys59=
NM_000031.5:c.177G=	NP_000022.3:p.Lys59=
NM_001003945.2:c.264G=	NP_001003945.1:p.Lys88=
NM_001003945.3:c.264G=	NP_001003945.1:p.Lys88=
NM_001317745.1:c.153G=	NP_001304674.1:p.Lys51=
NM_001317745.2:c.153G=	NP_001304674.1:p.Lys51=
ENST00000409155.7:c.177G=	ENSP00000386284.3:p.Lys59=
ENST00000448137.5:c.204G=	ENSP00000392748.1:p.Lys68=
ENST00000464749.5:n.258-678G=
ENST00000468504.5:n.299G=
ENST00000482001.1:n.450G=
ENST00000482847.5:n.450G=
XM_005251799.1:c.264G=	XP_005251856.1:p.Lys88=
XM_011518363.1:c.303G=	XP_011516665.1:p.Lys101=
XM_011518364.1:c.204G=	XP_011516666.1:p.Lys68=
XM_011518364.2:c.204G=	XP_011516666.1:p.Lys68=
XM_024447449.1:c.264G=	XP_024303217.1:p.Lys88=
XR_002956764.1:n.677G=