Canonical Allele Identifier: CA411366379
Gene: APOL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.36265230A>T , CM000684.2:g.36265230A>T GRCh38
NC_000022.10:g.36661276A>T , CM000684.1:g.36661276A>T GRCh37
NC_000022.9:g.34991222A>T NCBI36
NG_023228.1:g.17160A>T , LRG_169:g.17160A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000427990.6:c.394A>T ENSP00000391302.2:p.Lys132Ter
ENST00000433768.6:c.*156A>T ENSP00000392514.1:n.*156A>T
ENST00000438034.6:c.481A>T ENSP00000404525.2:p.Lys161Ter
ENST00000397278.8:c.394A>T MANE Select ENSP00000380448.4:p.Lys132Ter
ENST00000319136.8:c.442A>T ENSP00000317674.4:p.Lys148Ter
ENST00000397278.7:c.394A>T ENSP00000380448.3:p.Lys132Ter
ENST00000397279.8:c.394A>T ENSP00000380449.4:p.Lys132Ter
ENST00000422706.5:c.394A>T ENSP00000411507.1:p.Lys132Ter
ENST00000426053.5:c.340A>T ENSP00000388477.1:p.Lys114Ter
ENST00000427990.5:c.394A>T ENSP00000391302.1:p.Lys132Ter
NM_001136540.1:c.394A>T NP_001130012.1:p.Lys132Ter
NM_001136541.1:c.340A>T NP_001130013.1:p.Lys114Ter
NM_003661.3:c.394A>T NP_003652.2:p.Lys132Ter
NM_145343.2:c.442A>T , LRG_169t1:c.442A>T NP_663318.1:p.Lys148Ter
XM_005261796.2:c.340A>T XP_005261853.1:p.Lys114Ter
XM_011530478.1:c.31A>T XP_011528780.1:p.Lys11Ter
NM_001362927.1:c.340A>T NP_001349856.1:p.Lys114Ter
XM_011530478.2:c.31A>T XP_011528780.1:p.Lys11Ter
NM_001362927.2:c.340A>T NP_001349856.1:p.Lys114Ter
NM_003661.4:c.394A>T MANE Select NP_003652.2:p.Lys132Ter
NM_001136540.2:c.394A>T NP_001130012.1:p.Lys132Ter
NM_001136541.2:c.340A>T NP_001130013.1:p.Lys114Ter
NM_145343.3:c.442A>T NP_663318.1:p.Lys148Ter