Canonical Allele Identifier: CA5196323
Gene: ALAD HGNC NCBI

Linked Data

dbSNP Id: rs373715261

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.113389031C>A , CM000671.2:g.113389031C>A GRCh38
NC_000009.11:g.116151311C>A , CM000671.1:g.116151311C>A GRCh37
NC_000009.10:g.115191132C>A NCBI36
NG_008716.1:g.17308G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000409155.8:c.877G>T MANE Select ENSP00000386284.3:p.Ala293Ser
ENST00000409155.7:c.877G>T ENSP00000386284.3:p.Ala293Ser
ENST00000482847.5:n.1150G>T
NM_000031.5:c.877G>T NP_000022.3:p.Ala293Ser
XM_005251799.1:c.964G>T XP_005251856.1:p.Ala322Ser
XM_011518363.1:c.1003G>T XP_011516665.1:p.Ala335Ser
XM_011518364.1:c.904G>T XP_011516666.1:p.Ala302Ser
NM_001003945.2:c.964G>T NP_001003945.1:p.Ala322Ser
NM_001317745.1:c.853G>T NP_001304674.1:p.Ala285Ser
XM_011518364.2:c.904G>T XP_011516666.1:p.Ala302Ser
XM_024447449.1:c.964G>T XP_024303217.1:p.Ala322Ser
NM_000031.6:c.877G>T MANE Select NP_000022.3:p.Ala293Ser
NM_001003945.3:c.964G>T NP_001003945.1:p.Ala322Ser
NM_001317745.2:c.853G>T NP_001304674.1:p.Ala285Ser