Canonical Allele Identifier: CA181104

Gene: APOL1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36265988T>G , CM000684.2:g.36265988T>G	GRCh38
NC_000022.10:g.36662034T>G , CM000684.1:g.36662034T>G	GRCh37
NC_000022.9:g.34991980T>G	NCBI36
NG_023228.1:g.17918T>G , LRG_169:g.17918T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427990.6:c.1152T>G	ENSP00000391302.2:p.Ile384Met
ENST00000433768.6:c.*914T>G	ENSP00000392514.1:n.*914T>G
ENST00000438034.6:c.1239T>G	ENSP00000404525.2:p.Ile413Met
ENST00000397278.8:c.1152T>G MANE Select	ENSP00000380448.4:p.Ile384Met
ENST00000319136.8:c.1200T>G	ENSP00000317674.4:p.Ile400Met
ENST00000397278.7:c.1152T>G	ENSP00000380448.3:p.Ile384Met
ENST00000397279.8:c.1152T>G	ENSP00000380449.4:p.Ile384Met
ENST00000422706.5:c.1152T>G	ENSP00000411507.1:p.Ile384Met
ENST00000426053.5:c.1098T>G	ENSP00000388477.1:p.Ile366Met
NM_001136540.1:c.1152T>G	NP_001130012.1:p.Ile384Met
NM_001136541.1:c.1098T>G	NP_001130013.1:p.Ile366Met
NM_003661.3:c.1152T>G	NP_003652.2:p.Ile384Met
NM_145343.2:c.1200T>G , LRG_169t1:c.1200T>G	NP_663318.1:p.Ile400Met
XM_005261796.2:c.1098T>G	XP_005261853.1:p.Ile366Met
XM_011530478.1:c.789T>G	XP_011528780.1:p.Ile263Met
NM_001362927.1:c.1098T>G	NP_001349856.1:p.Ile366Met
XM_011530478.2:c.789T>G	XP_011528780.1:p.Ile263Met
NM_001362927.2:c.1098T>G	NP_001349856.1:p.Ile366Met
NM_003661.4:c.1152T>G MANE Select	NP_003652.2:p.Ile384Met
NM_001136540.2:c.1152T>G	NP_001130012.1:p.Ile384Met
NM_001136541.2:c.1098T>G	NP_001130013.1:p.Ile366Met
NM_145343.3:c.1200T>G	NP_663318.1:p.Ile400Met