Canonical Allele Identifier: CA374562935

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116151275T>G (hg19) ; chr9:g.113388995T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113388995T>G , CM000671.2:g.113388995T>G	GRCh38
NC_000009.11:g.116151275T>G , CM000671.1:g.116151275T>G	GRCh37
NC_000009.10:g.115191096T>G	NCBI36
NG_008716.1:g.17344A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.913A>C MANE Select	ENSP00000386284.3:p.Thr305Pro
ENST00000409155.7:c.913A>C	ENSP00000386284.3:p.Thr305Pro
ENST00000482847.5:n.1186A>C
NM_000031.5:c.913A>C	NP_000022.3:p.Thr305Pro
XM_005251799.1:c.1000A>C	XP_005251856.1:p.Thr334Pro
XM_011518363.1:c.1039A>C	XP_011516665.1:p.Thr347Pro
XM_011518364.1:c.940A>C	XP_011516666.1:p.Thr314Pro
NM_001003945.2:c.1000A>C	NP_001003945.1:p.Thr334Pro
NM_001317745.1:c.889A>C	NP_001304674.1:p.Thr297Pro
XM_011518364.2:c.940A>C	XP_011516666.1:p.Thr314Pro
XM_024447449.1:c.1000A>C	XP_024303217.1:p.Thr334Pro
NM_000031.6:c.913A>C MANE Select	NP_000022.3:p.Thr305Pro
NM_001003945.3:c.1000A>C	NP_001003945.1:p.Thr334Pro
NM_001317745.2:c.889A>C	NP_001304674.1:p.Thr297Pro