Canonical Allele Identifier: CA2403785509

Gene: APOL1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36262809T= , CM000684.2:g.36262809T=	GRCh38
NC_000022.10:g.36658855T= , CM000684.1:g.36658855T=	GRCh37
NC_000022.9:g.34988801T=	NCBI36
NG_023228.1:g.14739T= , LRG_169:g.14739T=

Transcript Alleles

HGVS	Amino-acid Change
NM_003661.4:c.314+1087T= MANE Select	NP_003652.2:n.314+1087T=
ENST00000397278.8:c.314+1087T= MANE Select	ENSP00000380448.4:n.314+1087T=
NM_001136540.1:c.314+1087T=	NP_001130012.1:n.314+1087T=
NM_001136540.2:c.314+1087T=	NP_001130012.1:n.314+1087T=
NM_001136541.1:c.260+1087T=	NP_001130013.1:n.260+1087T=
NM_001136541.2:c.260+1087T=	NP_001130013.1:n.260+1087T=
NM_001362927.1:c.260+1087T=	NP_001349856.1:n.260+1087T=
NM_001362927.2:c.260+1087T=	NP_001349856.1:n.260+1087T=
NM_003661.3:c.314+1087T=	NP_003652.2:n.314+1087T=
NM_145343.2:c.362+1087T= , LRG_169t1:c.362+1087T=	NP_663318.1:n.362+1087T=
NM_145343.3:c.362+1087T=	NP_663318.1:n.362+1087T=
ENST00000319136.8:c.362+1087T=	ENSP00000317674.4:n.362+1087T=
ENST00000397278.7:c.314+1087T=	ENSP00000380448.3:n.314+1087T=
ENST00000397279.8:c.314+1087T=	ENSP00000380449.4:n.314+1087T=
ENST00000422706.5:c.314+1087T=	ENSP00000411507.1:n.314+1087T=
ENST00000426053.5:c.260+1087T=	ENSP00000388477.1:n.260+1087T=
ENST00000427990.5:c.314+1087T=	ENSP00000391302.1:n.314+1087T=
ENST00000427990.6:c.314+1087T=	ENSP00000391302.2:n.314+1087T=
ENST00000433768.6:c.*76+1087T=	ENSP00000392514.1:n.*76+1087T=
ENST00000438034.6:c.401+1087T=	ENSP00000404525.2:n.401+1087T=
XM_005261796.2:c.260+1087T=	XP_005261853.1:n.260+1087T=
XM_011530478.1:c.-50+1087T=	XP_011528780.1:n.-50+1087T=
XM_011530478.2:c.-50+1087T=	XP_011528780.1:n.-50+1087T=