Canonical Allele Identifier: CA374564939

Gene: ALAD

Linked Data

• MyVariant Identifiers: chr9:g.116153814A>C (hg19) ; chr9:g.113391534A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113391534A>C , CM000671.2:g.113391534A>C	GRCh38
NC_000009.11:g.116153814A>C , CM000671.1:g.116153814A>C	GRCh37
NC_000009.10:g.115193635A>C	NCBI36
NG_008716.1:g.14805T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000409155.8:c.254T>G MANE Select	ENSP00000386284.3:p.Val85Gly
ENST00000409155.7:c.254T>G	ENSP00000386284.3:p.Val85Gly
ENST00000448137.5:c.281T>G	ENSP00000392748.1:p.Val94Gly
ENST00000464749.5:n.258-601T>G
ENST00000468504.5:n.376T>G
ENST00000482001.1:n.527T>G
ENST00000482847.5:n.527T>G
NM_000031.5:c.254T>G	NP_000022.3:p.Val85Gly
XM_005251799.1:c.341T>G	XP_005251856.1:p.Val114Gly
XM_011518363.1:c.380T>G	XP_011516665.1:p.Val127Gly
XM_011518364.1:c.281T>G	XP_011516666.1:p.Val94Gly
NM_001003945.2:c.341T>G	NP_001003945.1:p.Val114Gly
NM_001317745.1:c.230T>G	NP_001304674.1:p.Val77Gly
XM_011518364.2:c.281T>G	XP_011516666.1:p.Val94Gly
XM_024447449.1:c.341T>G	XP_024303217.1:p.Val114Gly
XR_002956764.1:n.754T>G
NM_000031.6:c.254T>G MANE Select	NP_000022.3:p.Val85Gly
NM_001003945.3:c.341T>G	NP_001003945.1:p.Val114Gly
NM_001317745.2:c.230T>G	NP_001304674.1:p.Val77Gly