Canonical Allele Identifier: CA374565201

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116153896C>A (hg19) ; chr9:g.113391616C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391616C>A , CM000671.2:g.113391616C>A	GRCh38
NC_000009.11:g.116153896C>A , CM000671.1:g.116153896C>A	GRCh37
NC_000009.10:g.115193717C>A	NCBI36
NG_008716.1:g.14723G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.172G>T MANE Select	ENSP00000386284.3:p.Val58Leu
ENST00000409155.7:c.172G>T	ENSP00000386284.3:p.Val58Leu
ENST00000448137.5:c.199G>T	ENSP00000392748.1:p.Val67Leu
ENST00000464749.5:n.258-683G>T
ENST00000468504.5:n.294G>T
ENST00000482001.1:n.445G>T
ENST00000482847.5:n.445G>T
NM_000031.5:c.172G>T	NP_000022.3:p.Val58Leu
XM_005251799.1:c.259G>T	XP_005251856.1:p.Val87Leu
XM_011518363.1:c.298G>T	XP_011516665.1:p.Val100Leu
XM_011518364.1:c.199G>T	XP_011516666.1:p.Val67Leu
NM_001003945.2:c.259G>T	NP_001003945.1:p.Val87Leu
NM_001317745.1:c.148G>T	NP_001304674.1:p.Val50Leu
XM_011518364.2:c.199G>T	XP_011516666.1:p.Val67Leu
XM_024447449.1:c.259G>T	XP_024303217.1:p.Val87Leu
XR_002956764.1:n.672G>T
NM_000031.6:c.172G>T MANE Select	NP_000022.3:p.Val58Leu
NM_001003945.3:c.259G>T	NP_001003945.1:p.Val87Leu
NM_001317745.2:c.148G>T	NP_001304674.1:p.Val50Leu