Canonical Allele Identifier: CA1155655860

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16048733_16048734delinsCA , CM000663.2:g.16048733_16048734delinsCA	GRCh38
NC_000001.10:g.16375228_16375229delinsCA , CM000663.1:g.16375228_16375229delinsCA	GRCh37
NC_000001.9:g.16247815_16247816delinsCA	NCBI36
NG_013079.1:g.9982_9983delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.655+151_655+152delinsCA	ENSP00000507062.1:n.655+151_655+152delinsCA
ENST00000682793.1:c.655+151_655+152delinsCA	ENSP00000506910.1:n.655+151_655+152delinsCA
ENST00000682838.1:c.*313+151_*313+152delinsCA	ENSP00000507652.1:n.*313+151_*313+152delinsCA
ENST00000683578.1:c.655+151_655+152delinsCA	ENSP00000507430.1:n.655+151_655+152delinsCA
ENST00000683661.1:n.2190+151_2190+152delinsCA
ENST00000684324.1:c.655+151_655+152delinsCA	ENSP00000507937.1:n.655+151_655+152delinsCA
ENST00000684545.1:c.655+151_655+152delinsCA	ENSP00000506733.1:n.655+151_655+152delinsCA
ENST00000684714.1:c.655+151_655+152delinsCA	ENSP00000506861.1:n.655+151_655+152delinsCA
ENST00000684731.1:n.116+151_116+152delinsCA
ENST00000375679.9:c.655+151_655+152delinsCA MANE Select	ENSP00000364831.5:n.655+151_655+152delinsCA
ENST00000375679.8:c.655+151_655+152delinsCA	ENSP00000364831.4:n.655+151_655+152delinsCA
ENST00000619181.4:c.587+219_587+220delinsCA	ENSP00000483866.1:n.587+219_587+220delinsCA
NM_000085.4:c.655+151_655+152delinsCA	NP_000076.2:n.655+151_655+152delinsCA
XM_011540619.1:c.496+151_496+152delinsCA	XP_011538921.1:n.496+151_496+152delinsCA
XM_011540620.1:c.655+151_655+152delinsCA	XP_011538922.1:n.655+151_655+152delinsCA
NM_000085.5:c.655+151_655+152delinsCA MANE Select	NP_000076.2:n.655+151_655+152delinsCA