Canonical Allele Identifier: CA374563027

Gene: ALAD

Linked Data

• gnomAD v4: 9-113389040-G-C
• MyVariant Identifiers: chr9:g.116151320G>C (hg19) ; chr9:g.113389040G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389040G>C , CM000671.2:g.113389040G>C	GRCh38
NC_000009.11:g.116151320G>C , CM000671.1:g.116151320G>C	GRCh37
NC_000009.10:g.115191141G>C	NCBI36
NG_008716.1:g.17299C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.868C>G MANE Select	ENSP00000386284.3:p.Gln290Glu
ENST00000409155.7:c.868C>G	ENSP00000386284.3:p.Gln290Glu
ENST00000482847.5:n.1141C>G
NM_000031.5:c.868C>G	NP_000022.3:p.Gln290Glu
XM_005251799.1:c.955C>G	XP_005251856.1:p.Gln319Glu
XM_011518363.1:c.994C>G	XP_011516665.1:p.Gln332Glu
XM_011518364.1:c.895C>G	XP_011516666.1:p.Gln299Glu
NM_001003945.2:c.955C>G	NP_001003945.1:p.Gln319Glu
NM_001317745.1:c.844C>G	NP_001304674.1:p.Gln282Glu
XM_011518364.2:c.895C>G	XP_011516666.1:p.Gln299Glu
XM_024447449.1:c.955C>G	XP_024303217.1:p.Gln319Glu
NM_000031.6:c.868C>G MANE Select	NP_000022.3:p.Gln290Glu
NM_001003945.3:c.955C>G	NP_001003945.1:p.Gln319Glu
NM_001317745.2:c.844C>G	NP_001304674.1:p.Gln282Glu