Canonical Allele Identifier: CA1155655844

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16048727_16048728delinsGC , CM000663.2:g.16048727_16048728delinsGC	GRCh38
NC_000001.10:g.16375222_16375223delinsGC , CM000663.1:g.16375222_16375223delinsGC	GRCh37
NC_000001.9:g.16247809_16247810delinsGC	NCBI36
NG_013079.1:g.9976_9977delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.655+145_655+146delinsGC	ENSP00000507062.1:n.655+145_655+146delinsGC
ENST00000682793.1:c.655+145_655+146delinsGC	ENSP00000506910.1:n.655+145_655+146delinsGC
ENST00000682838.1:c.*313+145_*313+146delinsGC	ENSP00000507652.1:n.*313+145_*313+146delinsGC
ENST00000683578.1:c.655+145_655+146delinsGC	ENSP00000507430.1:n.655+145_655+146delinsGC
ENST00000683661.1:n.2190+145_2190+146delinsGC
ENST00000684324.1:c.655+145_655+146delinsGC	ENSP00000507937.1:n.655+145_655+146delinsGC
ENST00000684545.1:c.655+145_655+146delinsGC	ENSP00000506733.1:n.655+145_655+146delinsGC
ENST00000684714.1:c.655+145_655+146delinsGC	ENSP00000506861.1:n.655+145_655+146delinsGC
ENST00000684731.1:n.116+145_116+146delinsGC
ENST00000375679.9:c.655+145_655+146delinsGC MANE Select	ENSP00000364831.5:n.655+145_655+146delinsGC
ENST00000375679.8:c.655+145_655+146delinsGC	ENSP00000364831.4:n.655+145_655+146delinsGC
ENST00000619181.4:c.587+213_587+214delinsGC	ENSP00000483866.1:n.587+213_587+214delinsGC
NM_000085.4:c.655+145_655+146delinsGC	NP_000076.2:n.655+145_655+146delinsGC
XM_011540619.1:c.496+145_496+146delinsGC	XP_011538921.1:n.496+145_496+146delinsGC
XM_011540620.1:c.655+145_655+146delinsGC	XP_011538922.1:n.655+145_655+146delinsGC
NM_000085.5:c.655+145_655+146delinsGC MANE Select	NP_000076.2:n.655+145_655+146delinsGC