Canonical Allele Identifier: CA1873365581

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389010C= , CM000671.2:g.113389010C=	GRCh38
NC_000009.11:g.116151290C= , CM000671.1:g.116151290C=	GRCh37
NC_000009.10:g.115191111C=	NCBI36
NG_008716.1:g.17329G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.898G= MANE Select	ENSP00000386284.3:p.Val300=
ENST00000409155.7:c.898G=	ENSP00000386284.3:p.Val300=
ENST00000482847.5:n.1171G=
NM_000031.5:c.898G=	NP_000022.3:p.Val300=
XM_005251799.1:c.985G=	XP_005251856.1:p.Val329=
XM_011518363.1:c.1024G=	XP_011516665.1:p.Val342=
XM_011518364.1:c.925G=	XP_011516666.1:p.Val309=
NM_001003945.2:c.985G=	NP_001003945.1:p.Val329=
NM_001317745.1:c.874G=	NP_001304674.1:p.Val292=
XM_011518364.2:c.925G=	XP_011516666.1:p.Val309=
XM_024447449.1:c.985G=	XP_024303217.1:p.Val329=
NM_000031.6:c.898G= MANE Select	NP_000022.3:p.Val300=
NM_001003945.3:c.985G=	NP_001003945.1:p.Val329=
NM_001317745.2:c.874G=	NP_001304674.1:p.Val292=