Canonical Allele Identifier: CA2574230755

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16051404_16051415del , CM000663.2:g.16051404_16051415del	GRCh38
NC_000001.10:g.16377899_16377910del , CM000663.1:g.16377899_16377910del	GRCh37
NC_000001.9:g.16250486_16250497del	NCBI36
NG_013079.1:g.12653_12664del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1228-74_1228-63del	ENSP00000507062.1:n.1228-74_1228-63del
ENST00000682793.1:c.1228-74_1228-63del	ENSP00000506910.1:n.1228-74_1228-63del
ENST00000682838.1:c.*970-74_*970-63del	ENSP00000507652.1:n.*970-74_*970-63del
ENST00000683578.1:c.1228-74_1228-63del	ENSP00000507430.1:n.1228-74_1228-63del
ENST00000683606.1:n.843-74_843-63del
ENST00000683661.1:n.2763-74_2763-63del
ENST00000684324.1:c.1228-74_1228-63del	ENSP00000507937.1:n.1228-74_1228-63del
ENST00000684545.1:c.1228-74_1228-63del	ENSP00000506733.1:n.1228-74_1228-63del
ENST00000684624.1:n.605-74_605-63del
ENST00000684714.1:c.1228-74_1228-63del	ENSP00000506861.1:n.1228-74_1228-63del
ENST00000684731.1:n.689-74_689-63del
ENST00000375679.9:c.1228-74_1228-63del MANE Select	ENSP00000364831.5:n.1228-74_1228-63del
ENST00000375667.7:c.721-74_721-63del	ENSP00000364819.3:n.721-74_721-63del
ENST00000375679.8:c.1228-74_1228-63del	ENSP00000364831.4:n.1228-74_1228-63del
ENST00000619181.4:c.847-74_847-63del	ENSP00000483866.1:n.847-74_847-63del
NM_000085.4:c.1228-74_1228-63del	NP_000076.2:n.1228-74_1228-63del
NM_001165945.2:c.721-74_721-63del	NP_001159417.2:n.721-74_721-63del
XM_011540619.1:c.1069-74_1069-63del	XP_011538921.1:n.1069-74_1069-63del
XM_011540620.1:c.1228-74_1228-63del	XP_011538922.1:n.1228-74_1228-63del
XM_011540621.1:c.577-74_577-63del	XP_011538923.1:n.577-74_577-63del
NM_000085.5:c.1228-74_1228-63del MANE Select	NP_000076.2:n.1228-74_1228-63del