Canonical Allele Identifier: CA1873365584

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389016C= , CM000671.2:g.113389016C=	GRCh38
NC_000009.11:g.116151296C= , CM000671.1:g.116151296C=	GRCh37
NC_000009.10:g.115191117C=	NCBI36
NG_008716.1:g.17323G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.892G= MANE Select	ENSP00000386284.3:p.Ala298=
ENST00000409155.7:c.892G=	ENSP00000386284.3:p.Ala298=
ENST00000482847.5:n.1165G=
NM_000031.5:c.892G=	NP_000022.3:p.Ala298=
XM_005251799.1:c.979G=	XP_005251856.1:p.Ala327=
XM_011518363.1:c.1018G=	XP_011516665.1:p.Ala340=
XM_011518364.1:c.919G=	XP_011516666.1:p.Ala307=
NM_001003945.2:c.979G=	NP_001003945.1:p.Ala327=
NM_001317745.1:c.868G=	NP_001304674.1:p.Ala290=
XM_011518364.2:c.919G=	XP_011516666.1:p.Ala307=
XM_024447449.1:c.979G=	XP_024303217.1:p.Ala327=
NM_000031.6:c.892G= MANE Select	NP_000022.3:p.Ala298=
NM_001003945.3:c.979G=	NP_001003945.1:p.Ala327=
NM_001317745.2:c.868G=	NP_001304674.1:p.Ala290=