Canonical Allele Identifier: CA2577701914

Gene: APOL1

Linked Data

• gnomAD v4: 22-36265253-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36265256del , CM000684.2:g.36265256del	GRCh38
NC_000022.10:g.36661302del , CM000684.1:g.36661302del	GRCh37
NC_000022.9:g.34991248del	NCBI36
NG_023228.1:g.17186del , LRG_169:g.17186del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427990.6:c.420del	ENSP00000391302.2:p.Leu141Ter
ENST00000433768.6:c.*182del	ENSP00000392514.1:n.*182del
ENST00000438034.6:c.507del	ENSP00000404525.2:p.Leu170Ter
ENST00000397278.8:c.420del MANE Select	ENSP00000380448.4:p.Leu141Ter
ENST00000319136.8:c.468del	ENSP00000317674.4:p.Leu157Ter
ENST00000397278.7:c.420del	ENSP00000380448.3:p.Leu141Ter
ENST00000397279.8:c.420del	ENSP00000380449.4:p.Leu141Ter
ENST00000422706.5:c.420del	ENSP00000411507.1:p.Leu141Ter
ENST00000426053.5:c.366del	ENSP00000388477.1:p.Leu123Ter
ENST00000427990.5:c.420del	ENSP00000391302.1:p.Leu141Ter
NM_001136540.1:c.420del	NP_001130012.1:p.Leu141Ter
NM_001136541.1:c.366del	NP_001130013.1:p.Leu123Ter
NM_003661.3:c.420del	NP_003652.2:p.Leu141Ter
NM_145343.2:c.468del , LRG_169t1:c.468del	NP_663318.1:p.Leu157Ter
XM_005261796.2:c.366del	XP_005261853.1:p.Leu123Ter
XM_011530478.1:c.57del	XP_011528780.1:p.Leu20Ter
NM_001362927.1:c.366del	NP_001349856.1:p.Leu123Ter
XM_011530478.2:c.57del	XP_011528780.1:p.Leu20Ter
NM_001362927.2:c.366del	NP_001349856.1:p.Leu123Ter
NM_003661.4:c.420del MANE Select	NP_003652.2:p.Leu141Ter
NM_001136540.2:c.420del	NP_001130012.1:p.Leu141Ter
NM_001136541.2:c.366del	NP_001130013.1:p.Leu123Ter
NM_145343.3:c.468del	NP_663318.1:p.Leu157Ter