Canonical Allele Identifier: CA1873365619
Gene: ALAD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.113389095G= , CM000671.2:g.113389095G= GRCh38
NC_000009.11:g.116151375G= , CM000671.1:g.116151375G= GRCh37
NC_000009.10:g.115191196G= NCBI36
NG_008716.1:g.17244C=

Transcript Alleles

HGVS Amino-acid change
ENST00000409155.8:c.813C= MANE Select ENSP00000386284.3:p.Leu271=
ENST00000409155.7:c.813C= ENSP00000386284.3:p.Leu271=
ENST00000482847.5:n.1086C=
NM_000031.5:c.813C= NP_000022.3:p.Leu271=
XM_005251799.1:c.900C= XP_005251856.1:p.Leu300=
XM_011518363.1:c.939C= XP_011516665.1:p.Leu313=
XM_011518364.1:c.840C= XP_011516666.1:p.Leu280=
NM_001003945.2:c.900C= NP_001003945.1:p.Leu300=
NM_001317745.1:c.789C= NP_001304674.1:p.Leu263=
XM_011518364.2:c.840C= XP_011516666.1:p.Leu280=
XM_024447449.1:c.900C= XP_024303217.1:p.Leu300=
NM_000031.6:c.813C= MANE Select NP_000022.3:p.Leu271=
NM_001003945.3:c.900C= NP_001003945.1:p.Leu300=
NM_001317745.2:c.789C= NP_001304674.1:p.Leu263=