Canonical Allele Identifier: CA466756308

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116151372A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389092A>C , CM000671.2:g.113389092A>C	GRCh38
NC_000009.11:g.116151372A>C , CM000671.1:g.116151372A>C	GRCh37
NC_000009.10:g.115191193A>C	NCBI36
NG_008716.1:g.17247T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.816T>G MANE Select	ENSP00000386284.3:p.Pro272=
ENST00000409155.7:c.816T>G	ENSP00000386284.3:p.Pro272=
ENST00000482847.5:n.1089T>G
NM_000031.5:c.816T>G	NP_000022.3:p.Pro272=
XM_005251799.1:c.903T>G	XP_005251856.1:p.Pro301=
XM_011518363.1:c.942T>G	XP_011516665.1:p.Pro314=
XM_011518364.1:c.843T>G	XP_011516666.1:p.Pro281=
NM_001003945.2:c.903T>G	NP_001003945.1:p.Pro301=
NM_001317745.1:c.792T>G	NP_001304674.1:p.Pro264=
XM_011518364.2:c.843T>G	XP_011516666.1:p.Pro281=
XM_024447449.1:c.903T>G	XP_024303217.1:p.Pro301=
NM_000031.6:c.816T>G MANE Select	NP_000022.3:p.Pro272=
NM_001003945.3:c.903T>G	NP_001003945.1:p.Pro301=
NM_001317745.2:c.792T>G	NP_001304674.1:p.Pro264=