Canonical Allele Identifier: CA466758209

Gene: ALAD

Linked Data

• gnomAD v4: 9-113391548-G-T
• MyVariant Identifiers: chr9:g.116153828G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391548G>T , CM000671.2:g.113391548G>T	GRCh38
NC_000009.11:g.116153828G>T , CM000671.1:g.116153828G>T	GRCh37
NC_000009.10:g.115193649G>T	NCBI36
NG_008716.1:g.14791C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.240C>A MANE Select	ENSP00000386284.3:p.Gly80=
ENST00000409155.7:c.240C>A	ENSP00000386284.3:p.Gly80=
ENST00000448137.5:c.267C>A	ENSP00000392748.1:p.Gly89=
ENST00000464749.5:n.258-615C>A
ENST00000468504.5:n.362C>A
ENST00000482001.1:n.513C>A
ENST00000482847.5:n.513C>A
NM_000031.5:c.240C>A	NP_000022.3:p.Gly80=
XM_005251799.1:c.327C>A	XP_005251856.1:p.Gly109=
XM_011518363.1:c.366C>A	XP_011516665.1:p.Gly122=
XM_011518364.1:c.267C>A	XP_011516666.1:p.Gly89=
NM_001003945.2:c.327C>A	NP_001003945.1:p.Gly109=
NM_001317745.1:c.216C>A	NP_001304674.1:p.Gly72=
XM_011518364.2:c.267C>A	XP_011516666.1:p.Gly89=
XM_024447449.1:c.327C>A	XP_024303217.1:p.Gly109=
XR_002956764.1:n.740C>A
NM_000031.6:c.240C>A MANE Select	NP_000022.3:p.Gly80=
NM_001003945.3:c.327C>A	NP_001003945.1:p.Gly109=
NM_001317745.2:c.216C>A	NP_001304674.1:p.Gly72=