Canonical Allele Identifier: CA1155658726

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16052024_16052027delinsGCCT , CM000663.2:g.16052024_16052027delinsGCCT	GRCh38
NC_000001.10:g.16378519_16378522delinsGCCT , CM000663.1:g.16378519_16378522delinsGCCT	GRCh37
NC_000001.9:g.16251106_16251109delinsGCCT	NCBI36
NG_013079.1:g.13273_13276delinsGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1409-174_1409-171delinsGCCT	ENSP00000507062.1:n.1409-174_1409-171delinsGCCT
ENST00000682793.1:c.1409-174_1409-171delinsGCCT	ENSP00000506910.1:n.1409-174_1409-171delinsGCCT
ENST00000682838.1:c.*1151-174_*1151-171delinsGCCT	ENSP00000507652.1:n.*1151-174_*1151-171delinsGCCT
ENST00000683578.1:c.1409-174_1409-171delinsGCCT	ENSP00000507430.1:n.1409-174_1409-171delinsGCCT
ENST00000683606.1:n.1024-183_1024-180delinsGCCT
ENST00000683661.1:n.2944-174_2944-171delinsGCCT
ENST00000684324.1:c.1409-174_1409-171delinsGCCT	ENSP00000507937.1:n.1409-174_1409-171delinsGCCT
ENST00000684545.1:c.1409-174_1409-171delinsGCCT	ENSP00000506733.1:n.1409-174_1409-171delinsGCCT
ENST00000684624.1:n.786-174_786-171delinsGCCT
ENST00000684714.1:c.1409-174_1409-171delinsGCCT	ENSP00000506861.1:n.1409-174_1409-171delinsGCCT
ENST00000684731.1:n.870-174_870-171delinsGCCT
ENST00000375679.9:c.1409-174_1409-171delinsGCCT MANE Select	ENSP00000364831.5:n.1409-174_1409-171delinsGCCT
ENST00000375667.7:c.902-174_902-171delinsGCCT	ENSP00000364819.3:n.902-174_902-171delinsGCCT
ENST00000375679.8:c.1409-174_1409-171delinsGCCT	ENSP00000364831.4:n.1409-174_1409-171delinsGCCT
ENST00000619181.4:c.1028-174_1028-171delinsGCCT	ENSP00000483866.1:n.1028-174_1028-171delinsGCCT
NM_000085.4:c.1409-174_1409-171delinsGCCT	NP_000076.2:n.1409-174_1409-171delinsGCCT
NM_001165945.2:c.902-174_902-171delinsGCCT	NP_001159417.2:n.902-174_902-171delinsGCCT
XM_011540619.1:c.1250-174_1250-171delinsGCCT	XP_011538921.1:n.1250-174_1250-171delinsGCCT
XM_011540620.1:c.1409-174_1409-171delinsGCCT	XP_011538922.1:n.1409-174_1409-171delinsGCCT
XM_011540621.1:c.758-174_758-171delinsGCCT	XP_011538923.1:n.758-174_758-171delinsGCCT
NM_000085.5:c.1409-174_1409-171delinsGCCT MANE Select	NP_000076.2:n.1409-174_1409-171delinsGCCT