Canonical Allele Identifier: CA10208680
Gene: APOL1 HGNC NCBI

Linked Data

dbSNP Id: rs2239785

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36265284G>A , CM000684.2:g.36265284G>A GRCh38
NC_000022.10:g.36661330G>A , CM000684.1:g.36661330G>A GRCh37
NC_000022.9:g.34991276G>A NCBI36
NG_023228.1:g.17214G>A , LRG_169:g.17214G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000319136.8:c.496G>A ENSP00000317674.4:p.Glu166Lys
ENST00000397278.7:c.448G>A ENSP00000380448.3:p.Glu150Lys
ENST00000397279.8:c.448G>A ENSP00000380449.4:p.Glu150Lys
ENST00000422706.5:c.448G>A ENSP00000411507.1:p.Glu150Lys
ENST00000426053.5:c.394G>A ENSP00000388477.1:p.Glu132Lys
ENST00000427990.5:c.448G>A ENSP00000391302.1:p.Glu150Lys
NM_001136540.1:c.448G>A NP_001130012.1:p.Glu150Lys
NM_001136541.1:c.394G>A NP_001130013.1:p.Glu132Lys
NM_003661.3:c.448G>A NP_003652.2:p.Glu150Lys
NM_145343.2:c.496G>A , LRG_169t1:c.496G>A NP_663318.1:p.Glu166Lys
XM_005261796.2:c.394G>A XP_005261853.1:p.Glu132Lys
XM_011530478.1:c.85G>A XP_011528780.1:p.Glu29Lys
NM_001362927.1:c.394G>A NP_001349856.1:p.Glu132Lys
XM_011530478.2:c.85G>A XP_011528780.1:p.Glu29Lys
NM_001362927.2:c.394G>A NP_001349856.1:p.Glu132Lys
NM_003661.4:c.448G>A MANE Select NP_003652.2:p.Glu150Lys
NM_001136540.2:c.448G>A NP_001130012.1:p.Glu150Lys
NM_001136541.2:c.394G>A NP_001130013.1:p.Glu132Lys