Canonical Allele Identifier: CA338644679
Gene: CLCNKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16055456T>A , CM000663.2:g.16055456T>A GRCh38
NC_000001.10:g.16381951T>A , CM000663.1:g.16381951T>A GRCh37
NC_000001.9:g.16254538T>A NCBI36
NG_013079.1:g.16705T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682338.1:c.1778T>A ENSP00000507062.1:p.Ile593Lys
ENST00000682793.1:c.1778T>A ENSP00000506910.1:p.Ile593Lys
ENST00000682838.1:c.*1520T>A ENSP00000507652.1:n.*1520T>A
ENST00000683578.1:c.1778T>A ENSP00000507430.1:p.Ile593Lys
ENST00000683606.1:n.1384T>A
ENST00000683661.1:n.3313T>A
ENST00000684324.1:c.1778T>A ENSP00000507937.1:p.Ile593Lys
ENST00000684545.1:c.1778T>A ENSP00000506733.1:p.Ile593Lys
ENST00000684624.1:n.1155T>A
ENST00000684714.1:c.1729T>A ENSP00000506861.1:p.Ter577Lys
ENST00000684731.1:n.1105T>A
ENST00000375679.9:c.1778T>A MANE Select ENSP00000364831.5:p.Ile593Lys
ENST00000375667.7:c.1271T>A ENSP00000364819.3:p.Ile424Lys
ENST00000375679.8:c.1778T>A ENSP00000364831.4:p.Ile593Lys
ENST00000431772.1:c.245T>A ENSP00000389344.1:p.Ile82Lys
ENST00000619181.4:c.1294-1731T>A ENSP00000483866.1:n.1294-1731T>A
NM_000085.4:c.1778T>A NP_000076.2:p.Ile593Lys
NM_001165945.2:c.1271T>A NP_001159417.2:p.Ile424Lys
XM_011540619.1:c.1619T>A XP_011538921.1:p.Ile540Lys
XM_011540621.1:c.1127T>A XP_011538923.1:p.Ile376Lys
NM_000085.5:c.1778T>A MANE Select NP_000076.2:p.Ile593Lys