Canonical Allele Identifier: CA1155625785

Gene: CLCNKA

Linked Data

• dbSNP Id: rs2022270248

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024575_16024576insT , CM000663.2:g.16024575_16024576insT	GRCh38
NC_000001.10:g.16351070_16351071insT , CM000663.1:g.16351070_16351071insT	GRCh37
NC_000001.9:g.16223657_16223658insT	NCBI36
NG_009359.1:g.7585_7586insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.230-188_230-187insT MANE Select	ENSP00000332771.4:n.230-188_230-187insT
ENST00000331433.4:c.230-188_230-187insT	ENSP00000332771.4:n.230-188_230-187insT
ENST00000375692.5:c.230-188_230-187insT	ENSP00000364844.1:n.230-188_230-187insT
ENST00000439316.6:c.229+647_229+648insT	ENSP00000414445.2:n.229+647_229+648insT
ENST00000464764.5:n.889-284_889-283insT
ENST00000495784.1:n.388-188_388-187insT
NM_001042704.1:c.230-188_230-187insT	NP_001036169.1:n.230-188_230-187insT
NM_001257139.1:c.229+647_229+648insT	NP_001244068.1:n.229+647_229+648insT
NM_004070.3:c.230-188_230-187insT	NP_004061.3:n.230-188_230-187insT
NM_004070.4:c.230-188_230-187insT MANE Select	NP_004061.3:n.230-188_230-187insT
NM_001042704.2:c.230-188_230-187insT	NP_001036169.1:n.230-188_230-187insT
NM_001257139.2:c.229+647_229+648insT	NP_001244068.1:n.229+647_229+648insT