Canonical Allele Identifier: CA411366302
Gene: APOL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36265200A>C , CM000684.2:g.36265200A>C GRCh38
NC_000022.10:g.36661246A>C , CM000684.1:g.36661246A>C GRCh37
NC_000022.9:g.34991192A>C NCBI36
NG_023228.1:g.17130A>C , LRG_169:g.17130A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000427990.6:c.364A>C ENSP00000391302.2:p.Met122Leu
ENST00000433768.6:c.*126A>C ENSP00000392514.1:n.*126A>C
ENST00000438034.6:c.451A>C ENSP00000404525.2:p.Met151Leu
ENST00000397278.8:c.364A>C MANE Select ENSP00000380448.4:p.Met122Leu
ENST00000319136.8:c.412A>C ENSP00000317674.4:p.Met138Leu
ENST00000397278.7:c.364A>C ENSP00000380448.3:p.Met122Leu
ENST00000397279.8:c.364A>C ENSP00000380449.4:p.Met122Leu
ENST00000422706.5:c.364A>C ENSP00000411507.1:p.Met122Leu
ENST00000426053.5:c.310A>C ENSP00000388477.1:p.Met104Leu
ENST00000427990.5:c.364A>C ENSP00000391302.1:p.Met122Leu
NM_001136540.1:c.364A>C NP_001130012.1:p.Met122Leu
NM_001136541.1:c.310A>C NP_001130013.1:p.Met104Leu
NM_003661.3:c.364A>C NP_003652.2:p.Met122Leu
NM_145343.2:c.412A>C , LRG_169t1:c.412A>C NP_663318.1:p.Met138Leu
XM_005261796.2:c.310A>C XP_005261853.1:p.Met104Leu
XM_011530478.1:c.1A>C XP_011528780.1:p.Met1Leu
NM_001362927.1:c.310A>C NP_001349856.1:p.Met104Leu
XM_011530478.2:c.1A>C XP_011528780.1:p.Met1Leu
NM_001362927.2:c.310A>C NP_001349856.1:p.Met104Leu
NM_003661.4:c.364A>C MANE Select NP_003652.2:p.Met122Leu
NM_001136540.2:c.364A>C NP_001130012.1:p.Met122Leu
NM_001136541.2:c.310A>C NP_001130013.1:p.Met104Leu
NM_145343.3:c.412A>C NP_663318.1:p.Met138Leu