Canonical Allele Identifier: CA2513924637

Gene: CLCNKA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024963_16024964insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC , CM000663.2:g.16024963_16024964insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC	GRCh38
NC_000001.10:g.16351458_16351459insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC , CM000663.1:g.16351458_16351459insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC	GRCh37
NC_000001.9:g.16224045_16224046insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC	NCBI36
NG_009359.1:g.7973_7974insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.358+72_358+73insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC MANE Select	ENSP00000332771.4:n.358+72_358+73insAGGCCACGGCCGCCAGGGCCGCCGC...
ENST00000331433.4:c.358+72_358+73insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC	ENSP00000332771.4:n.358+72_358+73insAGGCCACGGCCGCCAGGGCCGCCGC...
ENST00000375692.5:c.358+72_358+73insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC	ENSP00000364844.1:n.358+72_358+73insAGGCCACGGCCGCCAGGGCCGCCGC...
ENST00000439316.6:c.229+1035_229+1036insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC	ENSP00000414445.2:n.229+1035_229+1036insAGGCCACGGCCGCCAGGGCCG...
ENST00000464764.5:n.921+72_921+73insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC
ENST00000495784.1:n.516+72_516+73insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC
NM_001042704.1:c.358+72_358+73insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC	NP_001036169.1:n.358+72_358+73insAGGCCACGGCCGCCAGGGCCGCCGCGAG...
NM_001257139.1:c.229+1035_229+1036insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC	NP_001244068.1:n.229+1035_229+1036insAGGCCACGGCCGCCAGGGCCGCCG...
NM_004070.3:c.358+72_358+73insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC	NP_004061.3:n.358+72_358+73insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGC...
NM_004070.4:c.358+72_358+73insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC MANE Select	NP_004061.3:n.358+72_358+73insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGC...
NM_001042704.2:c.358+72_358+73insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC	NP_001036169.1:n.358+72_358+73insAGGCCACGGCCGCCAGGGCCGCCGCGAG...
NM_001257139.2:c.229+1035_229+1036insAGGCCACGGCCGCCAGGGCCGCCGCGAGCGCGATGAGGGTGGACGAGCGCAGCGGGACGACGGACACCCACGGCGTCAGGCCGCGCATCACCATCATCCTGGTGTACATGCGGTGGTAGTAGCGCTCGAC	NP_001244068.1:n.229+1035_229+1036insAGGCCACGGCCGCCAGGGCCGCCG...