Canonical Allele Identifier: CA466758204

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116153822G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391542G>C , CM000671.2:g.113391542G>C	GRCh38
NC_000009.11:g.116153822G>C , CM000671.1:g.116153822G>C	GRCh37
NC_000009.10:g.115193643G>C	NCBI36
NG_008716.1:g.14797C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.246C>G MANE Select	ENSP00000386284.3:p.Pro82=
ENST00000409155.7:c.246C>G	ENSP00000386284.3:p.Pro82=
ENST00000448137.5:c.273C>G	ENSP00000392748.1:p.Pro91=
ENST00000464749.5:n.258-609C>G
ENST00000468504.5:n.368C>G
ENST00000482001.1:n.519C>G
ENST00000482847.5:n.519C>G
NM_000031.5:c.246C>G	NP_000022.3:p.Pro82=
XM_005251799.1:c.333C>G	XP_005251856.1:p.Pro111=
XM_011518363.1:c.372C>G	XP_011516665.1:p.Pro124=
XM_011518364.1:c.273C>G	XP_011516666.1:p.Pro91=
NM_001003945.2:c.333C>G	NP_001003945.1:p.Pro111=
NM_001317745.1:c.222C>G	NP_001304674.1:p.Pro74=
XM_011518364.2:c.273C>G	XP_011516666.1:p.Pro91=
XM_024447449.1:c.333C>G	XP_024303217.1:p.Pro111=
XR_002956764.1:n.746C>G
NM_000031.6:c.246C>G MANE Select	NP_000022.3:p.Pro82=
NM_001003945.3:c.333C>G	NP_001003945.1:p.Pro111=
NM_001317745.2:c.222C>G	NP_001304674.1:p.Pro74=