Canonical Allele Identifier: CA998973219

Gene: CLCNKB

Linked Data

• gnomAD v3: 1-16051626-G-GAGT
• gnomAD v4: 1-16051626-G-GAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16051626_16051627insAGT , CM000663.2:g.16051626_16051627insAGT	GRCh38
NC_000001.10:g.16378121_16378122insAGT , CM000663.1:g.16378121_16378122insAGT	GRCh37
NC_000001.9:g.16250708_16250709insAGT	NCBI36
NG_013079.1:g.12875_12876insAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1297+79_1297+80insAGT	ENSP00000507062.1:n.1297+79_1297+80insAGT
ENST00000682793.1:c.1297+79_1297+80insAGT	ENSP00000506910.1:n.1297+79_1297+80insAGT
ENST00000682838.1:c.*1039+79_*1039+80insAGT	ENSP00000507652.1:n.*1039+79_*1039+80insAGT
ENST00000683578.1:c.1297+79_1297+80insAGT	ENSP00000507430.1:n.1297+79_1297+80insAGT
ENST00000683606.1:n.912+79_912+80insAGT
ENST00000683661.1:n.2832+79_2832+80insAGT
ENST00000684324.1:c.1297+79_1297+80insAGT	ENSP00000507937.1:n.1297+79_1297+80insAGT
ENST00000684545.1:c.1297+79_1297+80insAGT	ENSP00000506733.1:n.1297+79_1297+80insAGT
ENST00000684624.1:n.674+79_674+80insAGT
ENST00000684714.1:c.1297+79_1297+80insAGT	ENSP00000506861.1:n.1297+79_1297+80insAGT
ENST00000684731.1:n.758+79_758+80insAGT
ENST00000375679.9:c.1297+79_1297+80insAGT MANE Select	ENSP00000364831.5:n.1297+79_1297+80insAGT
ENST00000375667.7:c.790+79_790+80insAGT	ENSP00000364819.3:n.790+79_790+80insAGT
ENST00000375679.8:c.1297+79_1297+80insAGT	ENSP00000364831.4:n.1297+79_1297+80insAGT
ENST00000619181.4:c.916+79_916+80insAGT	ENSP00000483866.1:n.916+79_916+80insAGT
NM_000085.4:c.1297+79_1297+80insAGT	NP_000076.2:n.1297+79_1297+80insAGT
NM_001165945.2:c.790+79_790+80insAGT	NP_001159417.2:n.790+79_790+80insAGT
XM_011540619.1:c.1138+79_1138+80insAGT	XP_011538921.1:n.1138+79_1138+80insAGT
XM_011540620.1:c.1297+79_1297+80insAGT	XP_011538922.1:n.1297+79_1297+80insAGT
XM_011540621.1:c.646+79_646+80insAGT	XP_011538923.1:n.646+79_646+80insAGT
NM_000085.5:c.1297+79_1297+80insAGT MANE Select	NP_000076.2:n.1297+79_1297+80insAGT