Canonical Allele Identifier: CA2742592253
Gene: CLCNKA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16024948_16024949insAAGCCAA , CM000663.2:g.16024948_16024949insAAGCCAA GRCh38
NC_000001.10:g.16351443_16351444insAAGCCAA , CM000663.1:g.16351443_16351444insAAGCCAA GRCh37
NC_000001.9:g.16224030_16224031insAAGCCAA NCBI36
NG_009359.1:g.7958_7959insAAGCCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000331433.5:c.358+57_358+58insAAGCCAA MANE Select ENSP00000332771.4:n.358+57_358+58insAAGCCAA
ENST00000331433.4:c.358+57_358+58insAAGCCAA ENSP00000332771.4:n.358+57_358+58insAAGCCAA
ENST00000375692.5:c.358+57_358+58insAAGCCAA ENSP00000364844.1:n.358+57_358+58insAAGCCAA
ENST00000439316.6:c.229+1020_229+1021insAAGCCAA ENSP00000414445.2:n.229+1020_229+1021insAAGCCAA
ENST00000464764.5:n.921+57_921+58insAAGCCAA
ENST00000495784.1:n.516+57_516+58insAAGCCAA
NM_001042704.1:c.358+57_358+58insAAGCCAA NP_001036169.1:n.358+57_358+58insAAGCCAA
NM_001257139.1:c.229+1020_229+1021insAAGCCAA NP_001244068.1:n.229+1020_229+1021insAAGCCAA
NM_004070.3:c.358+57_358+58insAAGCCAA NP_004061.3:n.358+57_358+58insAAGCCAA
NM_004070.4:c.358+57_358+58insAAGCCAA MANE Select NP_004061.3:n.358+57_358+58insAAGCCAA
NM_001042704.2:c.358+57_358+58insAAGCCAA NP_001036169.1:n.358+57_358+58insAAGCCAA
NM_001257139.2:c.229+1020_229+1021insAAGCCAA NP_001244068.1:n.229+1020_229+1021insAAGCCAA