Canonical Allele Identifier: CA14967817

Gene: APOL1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36266340T>C , CM000684.2:g.36266340T>C	GRCh38
NC_000022.10:g.36662386T>C , CM000684.1:g.36662386T>C	GRCh37
NC_000022.9:g.34992332T>C	NCBI36
NG_023228.1:g.18270T>C , LRG_169:g.18270T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427990.6:c.*307T>C	ENSP00000391302.2:n.*307T>C
ENST00000433768.6:c.*1266T>C	ENSP00000392514.1:n.*1266T>C
ENST00000438034.6:c.*307T>C	ENSP00000404525.2:n.*307T>C
ENST00000397278.8:c.*307T>C MANE Select	ENSP00000380448.4:n.*307T>C
ENST00000319136.8:c.*307T>C	ENSP00000317674.4:n.*307T>C
ENST00000397278.7:c.*307T>C	ENSP00000380448.3:n.*307T>C
ENST00000397279.8:c.*74+233T>C	ENSP00000380449.4:n.*74+233T>C
ENST00000422706.5:c.*307T>C	ENSP00000411507.1:n.*307T>C
ENST00000426053.5:c.*307T>C	ENSP00000388477.1:n.*307T>C
NM_001136540.1:c.*307T>C	NP_001130012.1:n.*307T>C
NM_001136541.1:c.*307T>C	NP_001130013.1:n.*307T>C
NM_003661.3:c.*307T>C	NP_003652.2:n.*307T>C
NM_145343.2:c.*307T>C , LRG_169t1:c.*307T>C	NP_663318.1:n.*307T>C
NM_001362927.1:c.*307T>C	NP_001349856.1:n.*307T>C
XM_011530478.2:c.*307T>C	XP_011528780.1:n.*307T>C
NM_001362927.2:c.*307T>C	NP_001349856.1:n.*307T>C
NM_003661.4:c.*307T>C MANE Select	NP_003652.2:n.*307T>C
NM_001136540.2:c.*307T>C	NP_001130012.1:n.*307T>C
NM_001136541.2:c.*307T>C	NP_001130013.1:n.*307T>C
NM_145343.3:c.*307T>C	NP_663318.1:n.*307T>C