Canonical Allele Identifier: CA1873366685

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391438A= , CM000671.2:g.113391438A=	GRCh38
NC_000009.11:g.116153718A= , CM000671.1:g.116153718A=	GRCh37
NC_000009.10:g.115193539A=	NCBI36
NG_008716.1:g.14901T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.261+89T= MANE Select	ENSP00000386284.3:n.261+89T=
ENST00000409155.7:c.261+89T=	ENSP00000386284.3:n.261+89T=
ENST00000448137.5:c.288+89T=	ENSP00000392748.1:n.288+89T=
ENST00000464749.5:n.258-505T=
ENST00000468504.5:n.383+89T=
ENST00000482001.1:n.534+89T=
ENST00000482847.5:n.534+89T=
NM_000031.5:c.261+89T=	NP_000022.3:n.261+89T=
XM_005251799.1:c.348+89T=	XP_005251856.1:n.348+89T=
XM_011518363.1:c.387+89T=	XP_011516665.1:n.387+89T=
XM_011518364.1:c.288+89T=	XP_011516666.1:n.288+89T=
NM_001003945.2:c.348+89T=	NP_001003945.1:n.348+89T=
NM_001317745.1:c.237+89T=	NP_001304674.1:n.237+89T=
XM_011518364.2:c.288+89T=	XP_011516666.1:n.288+89T=
XM_024447449.1:c.348+89T=	XP_024303217.1:n.348+89T=
XR_002956764.1:n.761+89T=
NM_000031.6:c.261+89T= MANE Select	NP_000022.3:n.261+89T=
NM_001003945.3:c.348+89T=	NP_001003945.1:n.348+89T=
NM_001317745.2:c.237+89T=	NP_001304674.1:n.237+89T=