Canonical Allele Identifier: CA2577701909

Gene: APOL1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36265089G>C , CM000684.2:g.36265089G>C	GRCh38
NC_000022.10:g.36661135G>C , CM000684.1:g.36661135G>C	GRCh37
NC_000022.9:g.34991081G>C	NCBI36
NG_023228.1:g.17019G>C , LRG_169:g.17019G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427990.6:c.315-62G>C	ENSP00000391302.2:n.315-62G>C
ENST00000433768.6:c.*77-62G>C	ENSP00000392514.1:n.*77-62G>C
ENST00000438034.6:c.402-62G>C	ENSP00000404525.2:n.402-62G>C
ENST00000397278.8:c.315-62G>C MANE Select	ENSP00000380448.4:n.315-62G>C
ENST00000319136.8:c.363-62G>C	ENSP00000317674.4:n.363-62G>C
ENST00000397278.7:c.315-62G>C	ENSP00000380448.3:n.315-62G>C
ENST00000397279.8:c.315-62G>C	ENSP00000380449.4:n.315-62G>C
ENST00000422706.5:c.315-62G>C	ENSP00000411507.1:n.315-62G>C
ENST00000426053.5:c.261-62G>C	ENSP00000388477.1:n.261-62G>C
ENST00000427990.5:c.315-62G>C	ENSP00000391302.1:n.315-62G>C
NM_001136540.1:c.315-62G>C	NP_001130012.1:n.315-62G>C
NM_001136541.1:c.261-62G>C	NP_001130013.1:n.261-62G>C
NM_003661.3:c.315-62G>C	NP_003652.2:n.315-62G>C
NM_145343.2:c.363-62G>C , LRG_169t1:c.363-62G>C	NP_663318.1:n.363-62G>C
XM_005261796.2:c.261-62G>C	XP_005261853.1:n.261-62G>C
XM_011530478.1:c.-49-62G>C	XP_011528780.1:n.-49-62G>C
NM_001362927.1:c.261-62G>C	NP_001349856.1:n.261-62G>C
XM_011530478.2:c.-49-62G>C	XP_011528780.1:n.-49-62G>C
NM_001362927.2:c.261-62G>C	NP_001349856.1:n.261-62G>C
NM_003661.4:c.315-62G>C MANE Select	NP_003652.2:n.315-62G>C
NM_001136540.2:c.315-62G>C	NP_001130012.1:n.315-62G>C
NM_001136541.2:c.261-62G>C	NP_001130013.1:n.261-62G>C
NM_145343.3:c.363-62G>C	NP_663318.1:n.363-62G>C