Canonical Allele Identifier: CA1873365528

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113388918G= , CM000671.2:g.113388918G=	GRCh38
NC_000009.11:g.116151198G= , CM000671.1:g.116151198G=	GRCh37
NC_000009.10:g.115191019G=	NCBI36
NG_008716.1:g.17421C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.931+59C= MANE Select	ENSP00000386284.3:n.931+59C=
ENST00000409155.7:c.931+59C=	ENSP00000386284.3:n.931+59C=
ENST00000482847.5:n.1204+59C=
NM_000031.5:c.931+59C=	NP_000022.3:n.931+59C=
XM_005251799.1:c.1018+59C=	XP_005251856.1:n.1018+59C=
XM_011518363.1:c.1057+59C=	XP_011516665.1:n.1057+59C=
XM_011518364.1:c.958+59C=	XP_011516666.1:n.958+59C=
NM_001003945.2:c.1018+59C=	NP_001003945.1:n.1018+59C=
NM_001317745.1:c.907+59C=	NP_001304674.1:n.907+59C=
XM_011518364.2:c.958+59C=	XP_011516666.1:n.958+59C=
XM_024447449.1:c.1018+59C=	XP_024303217.1:n.1018+59C=
NM_000031.6:c.931+59C= MANE Select	NP_000022.3:n.931+59C=
NM_001003945.3:c.1018+59C=	NP_001003945.1:n.1018+59C=
NM_001317745.2:c.907+59C=	NP_001304674.1:n.907+59C=