Canonical Allele Identifier: CA411367173

Gene: APOL1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36265600G>C , CM000684.2:g.36265600G>C	GRCh38
NC_000022.10:g.36661646G>C , CM000684.1:g.36661646G>C	GRCh37
NC_000022.9:g.34991592G>C	NCBI36
NG_023228.1:g.17530G>C , LRG_169:g.17530G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427990.6:c.764G>C	ENSP00000391302.2:p.Arg255Thr
ENST00000433768.6:c.*526G>C	ENSP00000392514.1:n.*526G>C
ENST00000438034.6:c.851G>C	ENSP00000404525.2:p.Arg284Thr
ENST00000397278.8:c.764G>C MANE Select	ENSP00000380448.4:p.Arg255Thr
ENST00000319136.8:c.812G>C	ENSP00000317674.4:p.Arg271Thr
ENST00000397278.7:c.764G>C	ENSP00000380448.3:p.Arg255Thr
ENST00000397279.8:c.764G>C	ENSP00000380449.4:p.Arg255Thr
ENST00000422706.5:c.764G>C	ENSP00000411507.1:p.Arg255Thr
ENST00000426053.5:c.710G>C	ENSP00000388477.1:p.Arg237Thr
NM_001136540.1:c.764G>C	NP_001130012.1:p.Arg255Thr
NM_001136541.1:c.710G>C	NP_001130013.1:p.Arg237Thr
NM_003661.3:c.764G>C	NP_003652.2:p.Arg255Thr
NM_145343.2:c.812G>C , LRG_169t1:c.812G>C	NP_663318.1:p.Arg271Thr
XM_005261796.2:c.710G>C	XP_005261853.1:p.Arg237Thr
XM_011530478.1:c.401G>C	XP_011528780.1:p.Arg134Thr
NM_001362927.1:c.710G>C	NP_001349856.1:p.Arg237Thr
XM_011530478.2:c.401G>C	XP_011528780.1:p.Arg134Thr
NM_001362927.2:c.710G>C	NP_001349856.1:p.Arg237Thr
NM_003661.4:c.764G>C MANE Select	NP_003652.2:p.Arg255Thr
NM_001136540.2:c.764G>C	NP_001130012.1:p.Arg255Thr
NM_001136541.2:c.710G>C	NP_001130013.1:p.Arg237Thr
NM_145343.3:c.812G>C	NP_663318.1:p.Arg271Thr