Canonical Allele Identifier: CA1873365594

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389038C= , CM000671.2:g.113389038C=	GRCh38
NC_000009.11:g.116151318C= , CM000671.1:g.116151318C=	GRCh37
NC_000009.10:g.115191139C=	NCBI36
NG_008716.1:g.17301G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.870G= MANE Select	ENSP00000386284.3:p.Gln290=
ENST00000409155.7:c.870G=	ENSP00000386284.3:p.Gln290=
ENST00000482847.5:n.1143G=
NM_000031.5:c.870G=	NP_000022.3:p.Gln290=
XM_005251799.1:c.957G=	XP_005251856.1:p.Gln319=
XM_011518363.1:c.996G=	XP_011516665.1:p.Gln332=
XM_011518364.1:c.897G=	XP_011516666.1:p.Gln299=
NM_001003945.2:c.957G=	NP_001003945.1:p.Gln319=
NM_001317745.1:c.846G=	NP_001304674.1:p.Gln282=
XM_011518364.2:c.897G=	XP_011516666.1:p.Gln299=
XM_024447449.1:c.957G=	XP_024303217.1:p.Gln319=
NM_000031.6:c.870G= MANE Select	NP_000022.3:p.Gln290=
NM_001003945.3:c.957G=	NP_001003945.1:p.Gln319=
NM_001317745.2:c.846G=	NP_001304674.1:p.Gln282=