Canonical Allele Identifier: CA2643569200

Gene: CLCNKB

Linked Data

• gnomAD v4: 1-16051386-TAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16051387_16051388del , CM000663.2:g.16051387_16051388del	GRCh38
NC_000001.10:g.16377882_16377883del , CM000663.1:g.16377882_16377883del	GRCh37
NC_000001.9:g.16250469_16250470del	NCBI36
NG_013079.1:g.12636_12637del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1228-91_1228-90del	ENSP00000507062.1:n.1228-91_1228-90del
ENST00000682793.1:c.1228-91_1228-90del	ENSP00000506910.1:n.1228-91_1228-90del
ENST00000682838.1:c.*970-91_*970-90del	ENSP00000507652.1:n.*970-91_*970-90del
ENST00000683578.1:c.1228-91_1228-90del	ENSP00000507430.1:n.1228-91_1228-90del
ENST00000683606.1:n.843-91_843-90del
ENST00000683661.1:n.2763-91_2763-90del
ENST00000684324.1:c.1228-91_1228-90del	ENSP00000507937.1:n.1228-91_1228-90del
ENST00000684545.1:c.1228-91_1228-90del	ENSP00000506733.1:n.1228-91_1228-90del
ENST00000684624.1:n.605-91_605-90del
ENST00000684714.1:c.1228-91_1228-90del	ENSP00000506861.1:n.1228-91_1228-90del
ENST00000684731.1:n.689-91_689-90del
ENST00000375679.9:c.1228-91_1228-90del MANE Select	ENSP00000364831.5:n.1228-91_1228-90del
ENST00000375667.7:c.721-91_721-90del	ENSP00000364819.3:n.721-91_721-90del
ENST00000375679.8:c.1228-91_1228-90del	ENSP00000364831.4:n.1228-91_1228-90del
ENST00000619181.4:c.847-91_847-90del	ENSP00000483866.1:n.847-91_847-90del
NM_000085.4:c.1228-91_1228-90del	NP_000076.2:n.1228-91_1228-90del
NM_001165945.2:c.721-91_721-90del	NP_001159417.2:n.721-91_721-90del
XM_011540619.1:c.1069-91_1069-90del	XP_011538921.1:n.1069-91_1069-90del
XM_011540620.1:c.1228-91_1228-90del	XP_011538922.1:n.1228-91_1228-90del
XM_011540621.1:c.577-91_577-90del	XP_011538923.1:n.577-91_577-90del
NM_000085.5:c.1228-91_1228-90del MANE Select	NP_000076.2:n.1228-91_1228-90del