Canonical Allele Identifier: CA14926082

Gene: APOL2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36234993T>C , CM000684.2:g.36234993T>C	GRCh38
NC_000022.10:g.36631039T>C , CM000684.1:g.36631039T>C	GRCh37
NC_000022.9:g.34960985T>C	NCBI36
NG_023229.2:g.9962A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358502.10:c.-133-1538A>G MANE Select	ENSP00000351292.5:n.-133-1538A>G
ENST00000249066.10:c.-133-1538A>G	ENSP00000249066.6:n.-133-1538A>G
ENST00000358502.9:c.-133-1538A>G	ENSP00000351292.5:n.-133-1538A>G
ENST00000451256.6:c.204-1538A>G	ENSP00000403153.2:n.204-1538A>G
ENST00000454728.5:c.-233-658A>G	ENSP00000400486.1:n.-233-658A>G
ENST00000529194.5:c.-133-1538A>G	ENSP00000431231.1:n.-133-1538A>G
NM_030882.3:c.-133-1538A>G	NP_112092.2:n.-133-1538A>G
NM_145637.2:c.-133-1538A>G	NP_663612.2:n.-133-1538A>G
XM_011530074.1:c.-133-1538A>G	XP_011528376.1:n.-133-1538A>G
XM_011530075.1:c.-133-1538A>G	XP_011528377.1:n.-133-1538A>G
XM_011530076.1:c.-233-658A>G	XP_011528378.1:n.-233-658A>G
XM_011530077.1:c.-133-1538A>G	XP_011528379.1:n.-133-1538A>G
XM_011530078.1:c.-233-658A>G	XP_011528380.1:n.-233-658A>G
XM_011530076.3:c.-233-658A>G	XP_011528378.1:n.-233-658A>G
XM_011530077.3:c.-133-1538A>G	XP_011528379.1:n.-133-1538A>G
XM_017028724.1:c.204-1538A>G	XP_016884213.1:n.204-1538A>G
NM_030882.4:c.-133-1538A>G MANE Select	NP_112092.2:n.-133-1538A>G
NM_145637.3:c.-133-1538A>G	NP_663612.2:n.-133-1538A>G