Canonical Allele Identifier: CA2643560302
Gene: CLCNKA HGNC NCBI

Linked Data

gnomAD v4: 1-16025034-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16025034A>G , CM000663.2:g.16025034A>G GRCh38
NC_000001.10:g.16351529A>G , CM000663.1:g.16351529A>G GRCh37
NC_000001.9:g.16224116A>G NCBI36
NG_009359.1:g.8044A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331433.5:c.358+143A>G MANE Select ENSP00000332771.4:n.358+143A>G
ENST00000331433.4:c.358+143A>G ENSP00000332771.4:n.358+143A>G
ENST00000375692.5:c.358+143A>G ENSP00000364844.1:n.358+143A>G
ENST00000439316.6:c.230-1074A>G ENSP00000414445.2:n.230-1074A>G
ENST00000464764.5:n.921+143A>G
ENST00000495784.1:n.516+143A>G
NM_001042704.1:c.358+143A>G NP_001036169.1:n.358+143A>G
NM_001257139.1:c.230-1074A>G NP_001244068.1:n.230-1074A>G
NM_004070.3:c.358+143A>G NP_004061.3:n.358+143A>G
NM_004070.4:c.358+143A>G MANE Select NP_004061.3:n.358+143A>G
NM_001042704.2:c.358+143A>G NP_001036169.1:n.358+143A>G
NM_001257139.2:c.230-1074A>G NP_001244068.1:n.230-1074A>G