Canonical Allele Identifier: CA1155626251
Gene: CLCNKA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16024781G= , CM000663.2:g.16024781G= GRCh38
NC_000001.10:g.16351276G= , CM000663.1:g.16351276G= GRCh37
NC_000001.9:g.16223863G= NCBI36
NG_009359.1:g.7791G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331433.5:c.248G= MANE Select ENSP00000332771.4:p.Arg83=
ENST00000331433.4:c.248G= ENSP00000332771.4:p.Arg83=
ENST00000375692.5:c.248G= ENSP00000364844.1:p.Arg83=
ENST00000439316.6:c.229+853G= ENSP00000414445.2:n.229+853G=
ENST00000464764.5:n.889-78G=
ENST00000495784.1:n.406G=
NM_001042704.1:c.248G= NP_001036169.1:p.Arg83=
NM_001257139.1:c.229+853G= NP_001244068.1:n.229+853G=
NM_004070.3:c.248G= NP_004061.3:p.Arg83=
NM_004070.4:c.248G= MANE Select NP_004061.3:p.Arg83=
NM_001042704.2:c.248G= NP_001036169.1:p.Arg83=
NM_001257139.2:c.229+853G= NP_001244068.1:n.229+853G=