Canonical Allele Identifier: CA2643559967

Gene: CLCNKA

Linked Data

• gnomAD v4: 1-16024642-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024645_16024646del , CM000663.2:g.16024645_16024646del	GRCh38
NC_000001.10:g.16351140_16351141del , CM000663.1:g.16351140_16351141del	GRCh37
NC_000001.9:g.16223727_16223728del	NCBI36
NG_009359.1:g.7655_7656del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.230-118_230-117del MANE Select	ENSP00000332771.4:n.230-118_230-117del
ENST00000331433.4:c.230-118_230-117del	ENSP00000332771.4:n.230-118_230-117del
ENST00000375692.5:c.230-118_230-117del	ENSP00000364844.1:n.230-118_230-117del
ENST00000439316.6:c.229+717_229+718del	ENSP00000414445.2:n.229+717_229+718del
ENST00000464764.5:n.889-214_889-213del
ENST00000495784.1:n.388-118_388-117del
NM_001042704.1:c.230-118_230-117del	NP_001036169.1:n.230-118_230-117del
NM_001257139.1:c.229+717_229+718del	NP_001244068.1:n.229+717_229+718del
NM_004070.3:c.230-118_230-117del	NP_004061.3:n.230-118_230-117del
NM_004070.4:c.230-118_230-117del MANE Select	NP_004061.3:n.230-118_230-117del
NM_001042704.2:c.230-118_230-117del	NP_001036169.1:n.230-118_230-117del
NM_001257139.2:c.229+717_229+718del	NP_001244068.1:n.229+717_229+718del