Canonical Allele Identifier: CA1873365582

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389011G= , CM000671.2:g.113389011G=	GRCh38
NC_000009.11:g.116151291G= , CM000671.1:g.116151291G=	GRCh37
NC_000009.10:g.115191112G=	NCBI36
NG_008716.1:g.17328C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.897C= MANE Select	ENSP00000386284.3:p.Ala299=
ENST00000409155.7:c.897C=	ENSP00000386284.3:p.Ala299=
ENST00000482847.5:n.1170C=
NM_000031.5:c.897C=	NP_000022.3:p.Ala299=
XM_005251799.1:c.984C=	XP_005251856.1:p.Ala328=
XM_011518363.1:c.1023C=	XP_011516665.1:p.Ala341=
XM_011518364.1:c.924C=	XP_011516666.1:p.Ala308=
NM_001003945.2:c.984C=	NP_001003945.1:p.Ala328=
NM_001317745.1:c.873C=	NP_001304674.1:p.Ala291=
XM_011518364.2:c.924C=	XP_011516666.1:p.Ala308=
XM_024447449.1:c.984C=	XP_024303217.1:p.Ala328=
NM_000031.6:c.897C= MANE Select	NP_000022.3:p.Ala299=
NM_001003945.3:c.984C=	NP_001003945.1:p.Ala328=
NM_001317745.2:c.873C=	NP_001304674.1:p.Ala291=