Canonical Allele Identifier: CA353702
Gene: APOL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 277678
dbSNP Id: rs73885319

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36265860A>G , CM000684.2:g.36265860A>G GRCh38
NC_000022.10:g.36661906A>G , CM000684.1:g.36661906A>G GRCh37
NC_000022.9:g.34991852A>G NCBI36
NG_023228.1:g.17790A>G , LRG_169:g.17790A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000427990.6:c.1024A>G ENSP00000391302.2:p.Ser342Gly
ENST00000433768.6:c.*786A>G ENSP00000392514.1:n.*786A>G
ENST00000438034.6:c.1111A>G ENSP00000404525.2:p.Ser371Gly
ENST00000397278.8:c.1024A>G MANE Select ENSP00000380448.4:p.Ser342Gly
ENST00000319136.8:c.1072A>G ENSP00000317674.4:p.Ser358Gly
ENST00000397278.7:c.1024A>G ENSP00000380448.3:p.Ser342Gly
ENST00000397279.8:c.1024A>G ENSP00000380449.4:p.Ser342Gly
ENST00000422706.5:c.1024A>G ENSP00000411507.1:p.Ser342Gly
ENST00000426053.5:c.970A>G ENSP00000388477.1:p.Ser324Gly
NM_001136540.1:c.1024A>G NP_001130012.1:p.Ser342Gly
NM_001136541.1:c.970A>G NP_001130013.1:p.Ser324Gly
NM_003661.3:c.1024A>G NP_003652.2:p.Ser342Gly
NM_145343.2:c.1072A>G , LRG_169t1:c.1072A>G NP_663318.1:p.Ser358Gly
XM_005261796.2:c.970A>G XP_005261853.1:p.Ser324Gly
XM_011530478.1:c.661A>G XP_011528780.1:p.Ser221Gly
NM_001362927.1:c.970A>G NP_001349856.1:p.Ser324Gly
XM_011530478.2:c.661A>G XP_011528780.1:p.Ser221Gly
NM_001362927.2:c.970A>G NP_001349856.1:p.Ser324Gly
NM_003661.4:c.1024A>G MANE Select NP_003652.2:p.Ser342Gly
NM_001136540.2:c.1024A>G NP_001130012.1:p.Ser342Gly
NM_001136541.2:c.970A>G NP_001130013.1:p.Ser324Gly
NM_145343.3:c.1072A>G NP_663318.1:p.Ser358Gly