Canonical Allele Identifier: CA2403786689

Gene: APOL1

Linked Data

• dbSNP Id: rs2016202250

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36265304_36265306del , CM000684.2:g.36265304_36265306del	GRCh38
NC_000022.10:g.36661350_36661352del , CM000684.1:g.36661350_36661352del	GRCh37
NC_000022.9:g.34991296_34991298del	NCBI36
NG_023228.1:g.17234_17236del , LRG_169:g.17234_17236del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427990.6:c.468_470del	ENSP00000391302.2:p.Arg157del
ENST00000433768.6:c.*230_*232del	ENSP00000392514.1:n.*230_*232del
ENST00000438034.6:c.555_557del	ENSP00000404525.2:p.Arg186del
ENST00000397278.8:c.468_470del MANE Select	ENSP00000380448.4:p.Arg157del
ENST00000319136.8:c.516_518del	ENSP00000317674.4:p.Arg173del
ENST00000397278.7:c.468_470del	ENSP00000380448.3:p.Arg157del
ENST00000397279.8:c.468_470del	ENSP00000380449.4:p.Arg157del
ENST00000422706.5:c.468_470del	ENSP00000411507.1:p.Arg157del
ENST00000426053.5:c.414_416del	ENSP00000388477.1:p.Arg139del
ENST00000427990.5:c.468_470del	ENSP00000391302.1:p.Arg157del
NM_001136540.1:c.468_470del	NP_001130012.1:p.Arg157del
NM_001136541.1:c.414_416del	NP_001130013.1:p.Arg139del
NM_003661.3:c.468_470del	NP_003652.2:p.Arg157del
NM_145343.2:c.516_518del , LRG_169t1:c.516_518del	NP_663318.1:p.Arg173del
XM_005261796.2:c.414_416del	XP_005261853.1:p.Arg139del
XM_011530478.1:c.105_107del	XP_011528780.1:p.Arg36del
NM_001362927.1:c.414_416del	NP_001349856.1:p.Arg139del
XM_011530478.2:c.105_107del	XP_011528780.1:p.Arg36del
NM_001362927.2:c.414_416del	NP_001349856.1:p.Arg139del
NM_003661.4:c.468_470del MANE Select	NP_003652.2:p.Arg157del
NM_001136540.2:c.468_470del	NP_001130012.1:p.Arg157del
NM_001136541.2:c.414_416del	NP_001130013.1:p.Arg139del
NM_145343.3:c.516_518del	NP_663318.1:p.Arg173del