Canonical Allele Identifier: CA374564987

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116153826A>C (hg19) ; chr9:g.113391546A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391546A>C , CM000671.2:g.113391546A>C	GRCh38
NC_000009.11:g.116153826A>C , CM000671.1:g.116153826A>C	GRCh37
NC_000009.10:g.115193647A>C	NCBI36
NG_008716.1:g.14793T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.242T>G MANE Select	ENSP00000386284.3:p.Val81Gly
ENST00000409155.7:c.242T>G	ENSP00000386284.3:p.Val81Gly
ENST00000448137.5:c.269T>G	ENSP00000392748.1:p.Val90Gly
ENST00000464749.5:n.258-613T>G
ENST00000468504.5:n.364T>G
ENST00000482001.1:n.515T>G
ENST00000482847.5:n.515T>G
NM_000031.5:c.242T>G	NP_000022.3:p.Val81Gly
XM_005251799.1:c.329T>G	XP_005251856.1:p.Val110Gly
XM_011518363.1:c.368T>G	XP_011516665.1:p.Val123Gly
XM_011518364.1:c.269T>G	XP_011516666.1:p.Val90Gly
NM_001003945.2:c.329T>G	NP_001003945.1:p.Val110Gly
NM_001317745.1:c.218T>G	NP_001304674.1:p.Val73Gly
XM_011518364.2:c.269T>G	XP_011516666.1:p.Val90Gly
XM_024447449.1:c.329T>G	XP_024303217.1:p.Val110Gly
XR_002956764.1:n.742T>G
NM_000031.6:c.242T>G MANE Select	NP_000022.3:p.Val81Gly
NM_001003945.3:c.329T>G	NP_001003945.1:p.Val110Gly
NM_001317745.2:c.218T>G	NP_001304674.1:p.Val73Gly