Canonical Allele Identifier: CA374564523
Gene: ALAD HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.116153078C>G (hg19) chr9:g.113390798C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.113390798C>G , CM000671.2:g.113390798C>G GRCh38
NC_000009.11:g.116153078C>G , CM000671.1:g.116153078C>G GRCh37
NC_000009.10:g.115192899C>G NCBI36
NG_008716.1:g.15541G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000409155.8:c.397G>C MANE Select ENSP00000386284.3:p.Gly133Arg
ENST00000409155.7:c.397G>C ENSP00000386284.3:p.Gly133Arg
ENST00000464749.5:n.393G>C
ENST00000468504.5:n.519G>C
ENST00000482847.5:n.670G>C
NM_000031.5:c.397G>C NP_000022.3:p.Gly133Arg
XM_005251799.1:c.484G>C XP_005251856.1:p.Gly162Arg
XM_011518363.1:c.523G>C XP_011516665.1:p.Gly175Arg
XM_011518364.1:c.424G>C XP_011516666.1:p.Gly142Arg
NM_001003945.2:c.484G>C NP_001003945.1:p.Gly162Arg
NM_001317745.1:c.373G>C NP_001304674.1:p.Gly125Arg
XM_011518364.2:c.424G>C XP_011516666.1:p.Gly142Arg
XM_024447449.1:c.484G>C XP_024303217.1:p.Gly162Arg
XR_002956764.1:n.897G>C
NM_000031.6:c.397G>C MANE Select NP_000022.3:p.Gly133Arg
NM_001003945.3:c.484G>C NP_001003945.1:p.Gly162Arg
NM_001317745.2:c.373G>C NP_001304674.1:p.Gly125Arg
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