Canonical Allele Identifier: CA1873365496

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113388858G= , CM000671.2:g.113388858G=	GRCh38
NC_000009.11:g.116151138G= , CM000671.1:g.116151138G=	GRCh37
NC_000009.10:g.115190959G=	NCBI36
NG_008716.1:g.17481C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.931+119C= MANE Select	ENSP00000386284.3:n.931+119C=
ENST00000409155.7:c.931+119C=	ENSP00000386284.3:n.931+119C=
ENST00000482847.5:n.1204+119C=
NM_000031.5:c.931+119C=	NP_000022.3:n.931+119C=
XM_005251799.1:c.1018+119C=	XP_005251856.1:n.1018+119C=
XM_011518363.1:c.1057+119C=	XP_011516665.1:n.1057+119C=
XM_011518364.1:c.958+119C=	XP_011516666.1:n.958+119C=
NM_001003945.2:c.1018+119C=	NP_001003945.1:n.1018+119C=
NM_001317745.1:c.907+119C=	NP_001304674.1:n.907+119C=
XM_011518364.2:c.958+119C=	XP_011516666.1:n.958+119C=
XM_024447449.1:c.1018+119C=	XP_024303217.1:n.1018+119C=
NM_000031.6:c.931+119C= MANE Select	NP_000022.3:n.931+119C=
NM_001003945.3:c.1018+119C=	NP_001003945.1:n.1018+119C=
NM_001317745.2:c.907+119C=	NP_001304674.1:n.907+119C=