Canonical Allele Identifier: CA2403784783

Gene: APOL1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36261386G= , CM000684.2:g.36261386G=	GRCh38
NC_000022.10:g.36657432G= , CM000684.1:g.36657432G=	GRCh37
NC_000022.9:g.34987378G=	NCBI36
NG_023228.1:g.13316G= , LRG_169:g.13316G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003661.4:c.188-210G= MANE Select	NP_003652.2:n.188-210G=
ENST00000397278.8:c.188-210G= MANE Select	ENSP00000380448.4:n.188-210G=
NM_001136540.1:c.188-210G=	NP_001130012.1:n.188-210G=
NM_001136540.2:c.188-210G=	NP_001130012.1:n.188-210G=
NM_001136541.1:c.134-210G=	NP_001130013.1:n.134-210G=
NM_001136541.2:c.134-210G=	NP_001130013.1:n.134-210G=
NM_001362927.1:c.134-210G=	NP_001349856.1:n.134-210G=
NM_001362927.2:c.134-210G=	NP_001349856.1:n.134-210G=
NM_003661.3:c.188-210G=	NP_003652.2:n.188-210G=
NM_145343.2:c.236-210G= , LRG_169t1:c.236-210G=	NP_663318.1:n.236-210G=
NM_145343.3:c.236-210G=	NP_663318.1:n.236-210G=
ENST00000319136.8:c.236-210G=	ENSP00000317674.4:n.236-210G=
ENST00000397278.7:c.188-210G=	ENSP00000380448.3:n.188-210G=
ENST00000397279.8:c.188-210G=	ENSP00000380449.4:n.188-210G=
ENST00000422471.5:c.376-210G=	ENSP00000391206.1:n.376-210G=
ENST00000422706.5:c.188-210G=	ENSP00000411507.1:n.188-210G=
ENST00000426053.5:c.134-210G=	ENSP00000388477.1:n.134-210G=
ENST00000427990.5:c.188-210G=	ENSP00000391302.1:n.188-210G=
ENST00000427990.6:c.188-210G=	ENSP00000391302.2:n.188-210G=
ENST00000431184.1:c.*9-210G=	ENSP00000392857.1:n.*9-210G=
ENST00000433768.5:c.376-210G=	ENSP00000392514.1:n.376-210G=
ENST00000433768.6:c.376-210G=	ENSP00000392514.1:n.376-210G=
ENST00000438034.5:c.275-210G=	ENSP00000404525.1:n.275-210G=
ENST00000438034.6:c.275-210G=	ENSP00000404525.2:n.275-210G=
ENST00000439680.5:c.322-210G=	ENSP00000397141.1:n.322-210G=
XM_005261796.2:c.134-210G=	XP_005261853.1:n.134-210G=
XM_011530478.1:c.-176-210G=	XP_011528780.1:n.-176-210G=
XM_011530478.2:c.-176-210G=	XP_011528780.1:n.-176-210G=