Canonical Allele Identifier: CA466754856

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116151273A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113388993A>G , CM000671.2:g.113388993A>G	GRCh38
NC_000009.11:g.116151273A>G , CM000671.1:g.116151273A>G	GRCh37
NC_000009.10:g.115191094A>G	NCBI36
NG_008716.1:g.17346T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.915T>C MANE Select	ENSP00000386284.3:p.Thr305=
ENST00000409155.7:c.915T>C	ENSP00000386284.3:p.Thr305=
ENST00000482847.5:n.1188T>C
NM_000031.5:c.915T>C	NP_000022.3:p.Thr305=
XM_005251799.1:c.1002T>C	XP_005251856.1:p.Thr334=
XM_011518363.1:c.1041T>C	XP_011516665.1:p.Thr347=
XM_011518364.1:c.942T>C	XP_011516666.1:p.Thr314=
NM_001003945.2:c.1002T>C	NP_001003945.1:p.Thr334=
NM_001317745.1:c.891T>C	NP_001304674.1:p.Thr297=
XM_011518364.2:c.942T>C	XP_011516666.1:p.Thr314=
XM_024447449.1:c.1002T>C	XP_024303217.1:p.Thr334=
NM_000031.6:c.915T>C MANE Select	NP_000022.3:p.Thr305=
NM_001003945.3:c.1002T>C	NP_001003945.1:p.Thr334=
NM_001317745.2:c.891T>C	NP_001304674.1:p.Thr297=