Canonical Allele Identifier: CA411366274

Gene: APOL1

Linked Data

• MyVariant Identifiers: chr22:g.36661234C>G (hg19) ; chr22:g.36265188C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36265188C>G , CM000684.2:g.36265188C>G	GRCh38
NC_000022.10:g.36661234C>G , CM000684.1:g.36661234C>G	GRCh37
NC_000022.9:g.34991180C>G	NCBI36
NG_023228.1:g.17118C>G , LRG_169:g.17118C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000427990.6:c.352C>G	ENSP00000391302.2:p.Leu118Val
ENST00000433768.6:c.*114C>G	ENSP00000392514.1:n.*114C>G
ENST00000438034.6:c.439C>G	ENSP00000404525.2:p.Leu147Val
ENST00000397278.8:c.352C>G MANE Select	ENSP00000380448.4:p.Leu118Val
ENST00000319136.8:c.400C>G	ENSP00000317674.4:p.Leu134Val
ENST00000397278.7:c.352C>G	ENSP00000380448.3:p.Leu118Val
ENST00000397279.8:c.352C>G	ENSP00000380449.4:p.Leu118Val
ENST00000422706.5:c.352C>G	ENSP00000411507.1:p.Leu118Val
ENST00000426053.5:c.298C>G	ENSP00000388477.1:p.Leu100Val
ENST00000427990.5:c.352C>G	ENSP00000391302.1:p.Leu118Val
NM_001136540.1:c.352C>G	NP_001130012.1:p.Leu118Val
NM_001136541.1:c.298C>G	NP_001130013.1:p.Leu100Val
NM_003661.3:c.352C>G	NP_003652.2:p.Leu118Val
NM_145343.2:c.400C>G , LRG_169t1:c.400C>G	NP_663318.1:p.Leu134Val
XM_005261796.2:c.298C>G	XP_005261853.1:p.Leu100Val
XM_011530478.1:c.-12C>G	XP_011528780.1:n.-12C>G
NM_001362927.1:c.298C>G	NP_001349856.1:p.Leu100Val
XM_011530478.2:c.-12C>G	XP_011528780.1:n.-12C>G
NM_001362927.2:c.298C>G	NP_001349856.1:p.Leu100Val
NM_003661.4:c.352C>G MANE Select	NP_003652.2:p.Leu118Val
NM_001136540.2:c.352C>G	NP_001130012.1:p.Leu118Val
NM_001136541.2:c.298C>G	NP_001130013.1:p.Leu100Val
NM_145343.3:c.400C>G	NP_663318.1:p.Leu134Val