Canonical Allele Identifier: CA514472703

Gene: APOL1

Linked Data

• MyVariant Identifiers: chr22:g.36661206A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36265160A>T , CM000684.2:g.36265160A>T	GRCh38
NC_000022.10:g.36661206A>T , CM000684.1:g.36661206A>T	GRCh37
NC_000022.9:g.34991152A>T	NCBI36
NG_023228.1:g.17090A>T , LRG_169:g.17090A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427990.6:c.324A>T	ENSP00000391302.2:p.Ala108=
ENST00000433768.6:c.*86A>T	ENSP00000392514.1:n.*86A>T
ENST00000438034.6:c.411A>T	ENSP00000404525.2:p.Ala137=
ENST00000397278.8:c.324A>T MANE Select	ENSP00000380448.4:p.Ala108=
ENST00000319136.8:c.372A>T	ENSP00000317674.4:p.Ala124=
ENST00000397278.7:c.324A>T	ENSP00000380448.3:p.Ala108=
ENST00000397279.8:c.324A>T	ENSP00000380449.4:p.Ala108=
ENST00000422706.5:c.324A>T	ENSP00000411507.1:p.Ala108=
ENST00000426053.5:c.270A>T	ENSP00000388477.1:p.Ala90=
ENST00000427990.5:c.324A>T	ENSP00000391302.1:p.Ala108=
NM_001136540.1:c.324A>T	NP_001130012.1:p.Ala108=
NM_001136541.1:c.270A>T	NP_001130013.1:p.Ala90=
NM_003661.3:c.324A>T	NP_003652.2:p.Ala108=
NM_145343.2:c.372A>T , LRG_169t1:c.372A>T	NP_663318.1:p.Ala124=
XM_005261796.2:c.270A>T	XP_005261853.1:p.Ala90=
XM_011530478.1:c.-40A>T	XP_011528780.1:n.-40A>T
NM_001362927.1:c.270A>T	NP_001349856.1:p.Ala90=
XM_011530478.2:c.-40A>T	XP_011528780.1:n.-40A>T
NM_001362927.2:c.270A>T	NP_001349856.1:p.Ala90=
NM_003661.4:c.324A>T MANE Select	NP_003652.2:p.Ala108=
NM_001136540.2:c.324A>T	NP_001130012.1:p.Ala108=
NM_001136541.2:c.270A>T	NP_001130013.1:p.Ala90=
NM_145343.3:c.372A>T	NP_663318.1:p.Ala124=