Canonical Allele Identifier: CA5196325

Gene: ALAD

Linked Data

• dbSNP Id: rs150649205
• ExAC: 9:116151312 C / T
• gnomAD v2: 9-116151312-C-T
• gnomAD v3: 9-113389032-C-T
• gnomAD v4: 9-113389032-C-T
• MyVariant Identifiers: chr9:g.116151312C>T (hg19) ; chr9:g.113389032C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389032C>T , CM000671.2:g.113389032C>T	GRCh38
NC_000009.11:g.116151312C>T , CM000671.1:g.116151312C>T	GRCh37
NC_000009.10:g.115191133C>T	NCBI36
NG_008716.1:g.17307G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.876G>A MANE Select	ENSP00000386284.3:p.Gly292=
ENST00000409155.7:c.876G>A	ENSP00000386284.3:p.Gly292=
ENST00000482847.5:n.1149G>A
NM_000031.5:c.876G>A	NP_000022.3:p.Gly292=
XM_005251799.1:c.963G>A	XP_005251856.1:p.Gly321=
XM_011518363.1:c.1002G>A	XP_011516665.1:p.Gly334=
XM_011518364.1:c.903G>A	XP_011516666.1:p.Gly301=
NM_001003945.2:c.963G>A	NP_001003945.1:p.Gly321=
NM_001317745.1:c.852G>A	NP_001304674.1:p.Gly284=
XM_011518364.2:c.903G>A	XP_011516666.1:p.Gly301=
XM_024447449.1:c.963G>A	XP_024303217.1:p.Gly321=
NM_000031.6:c.876G>A MANE Select	NP_000022.3:p.Gly292=
NM_001003945.3:c.963G>A	NP_001003945.1:p.Gly321=
NM_001317745.2:c.852G>A	NP_001304674.1:p.Gly284=