Canonical Allele Identifier: CA13091860

Gene: ALAD

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113400480C>T , CM000671.2:g.113400480C>T	GRCh38
NC_000009.11:g.116162760C>T , CM000671.1:g.116162760C>T	GRCh37
NC_000009.10:g.115202581C>T	NCBI36
NG_008716.1:g.5859G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.-76+732G>A MANE Select	ENSP00000386284.3:n.-76+732G>A
ENST00000409155.7:c.-76+732G>A	ENSP00000386284.3:n.-76+732G>A
ENST00000448137.5:c.-96+732G>A	ENSP00000392748.1:n.-96+732G>A
ENST00000464749.5:n.73+732G>A
ENST00000468504.5:n.47+732G>A
ENST00000482847.5:n.32+732G>A
ENST00000494848.1:n.73+732G>A
NM_000031.5:c.-76+732G>A	NP_000022.3:n.-76+732G>A
XM_005251799.1:c.-155+732G>A	XP_005251856.1:n.-155+732G>A
NM_001003945.2:c.-155+732G>A	NP_001003945.1:n.-155+732G>A
NM_001317745.1:c.-49+454G>A	NP_001304674.1:n.-49+454G>A
XM_011518364.2:c.-278+732G>A	XP_011516666.1:n.-278+732G>A
NM_000031.6:c.-76+732G>A MANE Select	NP_000022.3:n.-76+732G>A
NM_001003945.3:c.-155+732G>A	NP_001003945.1:n.-155+732G>A
NM_001317745.2:c.-49+454G>A	NP_001304674.1:n.-49+454G>A