Canonical Allele Identifier: CA2403786674

Gene: APOL1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36265271T= , CM000684.2:g.36265271T=	GRCh38
NC_000022.10:g.36661317T= , CM000684.1:g.36661317T=	GRCh37
NC_000022.9:g.34991263T=	NCBI36
NG_023228.1:g.17201T= , LRG_169:g.17201T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427990.6:c.435T=	ENSP00000391302.2:p.Pro145=
ENST00000433768.6:c.*197T=	ENSP00000392514.1:n.*197T=
ENST00000438034.6:c.522T=	ENSP00000404525.2:p.Pro174=
ENST00000397278.8:c.435T= MANE Select	ENSP00000380448.4:p.Pro145=
ENST00000319136.8:c.483T=	ENSP00000317674.4:p.Pro161=
ENST00000397278.7:c.435T=	ENSP00000380448.3:p.Pro145=
ENST00000397279.8:c.435T=	ENSP00000380449.4:p.Pro145=
ENST00000422706.5:c.435T=	ENSP00000411507.1:p.Pro145=
ENST00000426053.5:c.381T=	ENSP00000388477.1:p.Pro127=
ENST00000427990.5:c.435T=	ENSP00000391302.1:p.Pro145=
NM_001136540.1:c.435T=	NP_001130012.1:p.Pro145=
NM_001136541.1:c.381T=	NP_001130013.1:p.Pro127=
NM_003661.3:c.435T=	NP_003652.2:p.Pro145=
NM_145343.2:c.483T= , LRG_169t1:c.483T=	NP_663318.1:p.Pro161=
XM_005261796.2:c.381T=	XP_005261853.1:p.Pro127=
XM_011530478.1:c.72T=	XP_011528780.1:p.Pro24=
NM_001362927.1:c.381T=	NP_001349856.1:p.Pro127=
XM_011530478.2:c.72T=	XP_011528780.1:p.Pro24=
NM_001362927.2:c.381T=	NP_001349856.1:p.Pro127=
NM_003661.4:c.435T= MANE Select	NP_003652.2:p.Pro145=
NM_001136540.2:c.435T=	NP_001130012.1:p.Pro145=
NM_001136541.2:c.381T=	NP_001130013.1:p.Pro127=
NM_145343.3:c.483T=	NP_663318.1:p.Pro161=