Canonical Allele Identifier: CA14985519
Gene: APOL1 HGNC NCBI
gnomAD v4:

Genomic Alleles

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

Transcript Alleles

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