Canonical Allele Identifier: CA2403786660

Gene: APOL1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36265251_36265252delinsTG , CM000684.2:g.36265251_36265252delinsTG	GRCh38
NC_000022.10:g.36661297_36661298delinsTG , CM000684.1:g.36661297_36661298delinsTG	GRCh37
NC_000022.9:g.34991243_34991244delinsTG	NCBI36
NG_023228.1:g.17181_17182delinsTG , LRG_169:g.17181_17182delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427990.6:c.415_416delinsTG	ENSP00000391302.2:p.Trp139=
ENST00000433768.6:c.*177_*178delinsTG	ENSP00000392514.1:n.*177_*178delinsTG
ENST00000438034.6:c.502_503delinsTG	ENSP00000404525.2:p.Trp168=
ENST00000397278.8:c.415_416delinsTG MANE Select	ENSP00000380448.4:p.Trp139=
ENST00000319136.8:c.463_464delinsTG	ENSP00000317674.4:p.Trp155=
ENST00000397278.7:c.415_416delinsTG	ENSP00000380448.3:p.Trp139=
ENST00000397279.8:c.415_416delinsTG	ENSP00000380449.4:p.Trp139=
ENST00000422706.5:c.415_416delinsTG	ENSP00000411507.1:p.Trp139=
ENST00000426053.5:c.361_362delinsTG	ENSP00000388477.1:p.Trp121=
ENST00000427990.5:c.415_416delinsTG	ENSP00000391302.1:p.Trp139=
NM_001136540.1:c.415_416delinsTG	NP_001130012.1:p.Trp139=
NM_001136541.1:c.361_362delinsTG	NP_001130013.1:p.Trp121=
NM_003661.3:c.415_416delinsTG	NP_003652.2:p.Trp139=
NM_145343.2:c.463_464delinsTG , LRG_169t1:c.463_464delinsTG	NP_663318.1:p.Trp155=
XM_005261796.2:c.361_362delinsTG	XP_005261853.1:p.Trp121=
XM_011530478.1:c.52_53delinsTG	XP_011528780.1:p.Trp18=
NM_001362927.1:c.361_362delinsTG	NP_001349856.1:p.Trp121=
XM_011530478.2:c.52_53delinsTG	XP_011528780.1:p.Trp18=
NM_001362927.2:c.361_362delinsTG	NP_001349856.1:p.Trp121=
NM_003661.4:c.415_416delinsTG MANE Select	NP_003652.2:p.Trp139=
NM_001136540.2:c.415_416delinsTG	NP_001130012.1:p.Trp139=
NM_001136541.2:c.361_362delinsTG	NP_001130013.1:p.Trp121=
NM_145343.3:c.463_464delinsTG	NP_663318.1:p.Trp155=