Canonical Allele Identifier: CA1873366737

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391547C= , CM000671.2:g.113391547C=	GRCh38
NC_000009.11:g.116153827C= , CM000671.1:g.116153827C=	GRCh37
NC_000009.10:g.115193648C=	NCBI36
NG_008716.1:g.14792G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.241G= MANE Select	ENSP00000386284.3:p.Val81=
ENST00000409155.7:c.241G=	ENSP00000386284.3:p.Val81=
ENST00000448137.5:c.268G=	ENSP00000392748.1:p.Val90=
ENST00000464749.5:n.258-614G=
ENST00000468504.5:n.363G=
ENST00000482001.1:n.514G=
ENST00000482847.5:n.514G=
NM_000031.5:c.241G=	NP_000022.3:p.Val81=
XM_005251799.1:c.328G=	XP_005251856.1:p.Val110=
XM_011518363.1:c.367G=	XP_011516665.1:p.Val123=
XM_011518364.1:c.268G=	XP_011516666.1:p.Val90=
NM_001003945.2:c.328G=	NP_001003945.1:p.Val110=
NM_001317745.1:c.217G=	NP_001304674.1:p.Val73=
XM_011518364.2:c.268G=	XP_011516666.1:p.Val90=
XM_024447449.1:c.328G=	XP_024303217.1:p.Val110=
XR_002956764.1:n.741G=
NM_000031.6:c.241G= MANE Select	NP_000022.3:p.Val81=
NM_001003945.3:c.328G=	NP_001003945.1:p.Val110=
NM_001317745.2:c.217G=	NP_001304674.1:p.Val73=