Canonical Allele Identifier: CA1155626081

Gene: CLCNKA

Linked Data

• dbSNP Id: rs2022277143

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024733_16024737dup , CM000663.2:g.16024733_16024737dup	GRCh38
NC_000001.10:g.16351228_16351232dup , CM000663.1:g.16351228_16351232dup	GRCh37
NC_000001.9:g.16223815_16223819dup	NCBI36
NG_009359.1:g.7743_7747dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.230-30_230-26dup MANE Select	ENSP00000332771.4:n.230-30_230-26dup
ENST00000331433.4:c.230-30_230-26dup	ENSP00000332771.4:n.230-30_230-26dup
ENST00000375692.5:c.230-30_230-26dup	ENSP00000364844.1:n.230-30_230-26dup
ENST00000439316.6:c.229+805_229+809dup	ENSP00000414445.2:n.229+805_229+809dup
ENST00000464764.5:n.889-126_889-122dup
ENST00000495784.1:n.388-30_388-26dup
NM_001042704.1:c.230-30_230-26dup	NP_001036169.1:n.230-30_230-26dup
NM_001257139.1:c.229+805_229+809dup	NP_001244068.1:n.229+805_229+809dup
NM_004070.3:c.230-30_230-26dup	NP_004061.3:n.230-30_230-26dup
NM_004070.4:c.230-30_230-26dup MANE Select	NP_004061.3:n.230-30_230-26dup
NM_001042704.2:c.230-30_230-26dup	NP_001036169.1:n.230-30_230-26dup
NM_001257139.2:c.229+805_229+809dup	NP_001244068.1:n.229+805_229+809dup