Canonical Allele Identifier: CA338644825
Gene: CLCNKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16055489A>G , CM000663.2:g.16055489A>G GRCh38
NC_000001.10:g.16381984A>G , CM000663.1:g.16381984A>G GRCh37
NC_000001.9:g.16254571A>G NCBI36
NG_013079.1:g.16738A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000682338.1:c.1811A>G ENSP00000507062.1:p.Lys604Arg
ENST00000682793.1:c.1811A>G ENSP00000506910.1:p.Lys604Arg
ENST00000682838.1:c.*1553A>G ENSP00000507652.1:n.*1553A>G
ENST00000683578.1:c.1811A>G ENSP00000507430.1:p.Lys604Arg
ENST00000683606.1:n.1417A>G
ENST00000683661.1:n.3346A>G
ENST00000684324.1:c.1811A>G ENSP00000507937.1:p.Lys604Arg
ENST00000684545.1:c.1811A>G ENSP00000506733.1:p.Lys604Arg
ENST00000684624.1:n.1188A>G
ENST00000684714.1:c.*31A>G ENSP00000506861.1:n.*31A>G
ENST00000684731.1:n.1138A>G
ENST00000375679.9:c.1811A>G MANE Select ENSP00000364831.5:p.Lys604Arg
ENST00000375667.7:c.1304A>G ENSP00000364819.3:p.Lys435Arg
ENST00000375679.8:c.1811A>G ENSP00000364831.4:p.Lys604Arg
ENST00000431772.1:c.278A>G ENSP00000389344.1:p.Lys93Arg
ENST00000619181.4:c.1294-1698A>G ENSP00000483866.1:n.1294-1698A>G
NM_000085.4:c.1811A>G NP_000076.2:p.Lys604Arg
NM_001165945.2:c.1304A>G NP_001159417.2:p.Lys435Arg
XM_011540619.1:c.1652A>G XP_011538921.1:p.Lys551Arg
XM_011540621.1:c.1160A>G XP_011538923.1:p.Lys387Arg
NM_000085.5:c.1811A>G MANE Select NP_000076.2:p.Lys604Arg