Canonical Allele Identifier: CA338644833
Gene: CLCNKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16055490G>T , CM000663.2:g.16055490G>T GRCh38
NC_000001.10:g.16381985G>T , CM000663.1:g.16381985G>T GRCh37
NC_000001.9:g.16254572G>T NCBI36
NG_013079.1:g.16739G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682338.1:c.1812G>T ENSP00000507062.1:p.Lys604Asn
ENST00000682793.1:c.1812G>T ENSP00000506910.1:p.Lys604Asn
ENST00000682838.1:c.*1554G>T ENSP00000507652.1:n.*1554G>T
ENST00000683578.1:c.1812G>T ENSP00000507430.1:p.Lys604Asn
ENST00000683606.1:n.1418G>T
ENST00000683661.1:n.3347G>T
ENST00000684324.1:c.1812G>T ENSP00000507937.1:p.Lys604Asn
ENST00000684545.1:c.1812G>T ENSP00000506733.1:p.Lys604Asn
ENST00000684624.1:n.1189G>T
ENST00000684714.1:c.*32G>T ENSP00000506861.1:n.*32G>T
ENST00000684731.1:n.1139G>T
ENST00000375679.9:c.1812G>T MANE Select ENSP00000364831.5:p.Lys604Asn
ENST00000375667.7:c.1305G>T ENSP00000364819.3:p.Lys435Asn
ENST00000375679.8:c.1812G>T ENSP00000364831.4:p.Lys604Asn
ENST00000431772.1:c.279G>T ENSP00000389344.1:p.Lys93Asn
ENST00000619181.4:c.1294-1697G>T ENSP00000483866.1:n.1294-1697G>T
NM_000085.4:c.1812G>T NP_000076.2:p.Lys604Asn
NM_001165945.2:c.1305G>T NP_001159417.2:p.Lys435Asn
XM_011540619.1:c.1653G>T XP_011538921.1:p.Lys551Asn
XM_011540621.1:c.1161G>T XP_011538923.1:p.Lys387Asn
NM_000085.5:c.1812G>T MANE Select NP_000076.2:p.Lys604Asn