Canonical Allele Identifier: CA1873366738

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391548G= , CM000671.2:g.113391548G=	GRCh38
NC_000009.11:g.116153828G= , CM000671.1:g.116153828G=	GRCh37
NC_000009.10:g.115193649G=	NCBI36
NG_008716.1:g.14791C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.240C= MANE Select	ENSP00000386284.3:p.Gly80=
ENST00000409155.7:c.240C=	ENSP00000386284.3:p.Gly80=
ENST00000448137.5:c.267C=	ENSP00000392748.1:p.Gly89=
ENST00000464749.5:n.258-615C=
ENST00000468504.5:n.362C=
ENST00000482001.1:n.513C=
ENST00000482847.5:n.513C=
NM_000031.5:c.240C=	NP_000022.3:p.Gly80=
XM_005251799.1:c.327C=	XP_005251856.1:p.Gly109=
XM_011518363.1:c.366C=	XP_011516665.1:p.Gly122=
XM_011518364.1:c.267C=	XP_011516666.1:p.Gly89=
NM_001003945.2:c.327C=	NP_001003945.1:p.Gly109=
NM_001317745.1:c.216C=	NP_001304674.1:p.Gly72=
XM_011518364.2:c.267C=	XP_011516666.1:p.Gly89=
XM_024447449.1:c.327C=	XP_024303217.1:p.Gly109=
XR_002956764.1:n.740C=
NM_000031.6:c.240C= MANE Select	NP_000022.3:p.Gly80=
NM_001003945.3:c.327C=	NP_001003945.1:p.Gly109=
NM_001317745.2:c.216C=	NP_001304674.1:p.Gly72=