Canonical Allele Identifier: CA623332

Gene: CLCNKB

Linked Data

• dbSNP Id: rs745397698
• ExAC: 1:16374788 C / CA
• gnomAD v2: 1-16374788-C-CA
• gnomAD v3: 1-16048293-C-CA
• gnomAD v4: 1-16048293-C-CA
• MyVariant Identifiers: chr1:g.16374788_16374789insA (hg19) ; chr1:g.16048293_16048294insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16048293_16048294insA , CM000663.2:g.16048293_16048294insA	GRCh38
NC_000001.10:g.16374788_16374789insA , CM000663.1:g.16374788_16374789insA	GRCh37
NC_000001.9:g.16247375_16247376insA	NCBI36
NG_013079.1:g.9542_9543insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.499-50_499-49insA	ENSP00000507062.1:n.499-50_499-49insA
ENST00000682793.1:c.499-50_499-49insA	ENSP00000506910.1:n.499-50_499-49insA
ENST00000682838.1:c.*157-50_*157-49insA	ENSP00000507652.1:n.*157-50_*157-49insA
ENST00000683578.1:c.499-50_499-49insA	ENSP00000507430.1:n.499-50_499-49insA
ENST00000683661.1:n.2034-50_2034-49insA
ENST00000684324.1:c.499-50_499-49insA	ENSP00000507937.1:n.499-50_499-49insA
ENST00000684545.1:c.499-50_499-49insA	ENSP00000506733.1:n.499-50_499-49insA
ENST00000684714.1:c.499-50_499-49insA	ENSP00000506861.1:n.499-50_499-49insA
ENST00000375679.9:c.499-50_499-49insA MANE Select	ENSP00000364831.5:n.499-50_499-49insA
ENST00000375679.8:c.499-50_499-49insA	ENSP00000364831.4:n.499-50_499-49insA
ENST00000619181.4:c.499-50_499-49insA	ENSP00000483866.1:n.499-50_499-49insA
NM_000085.4:c.499-50_499-49insA	NP_000076.2:n.499-50_499-49insA
XM_011540619.1:c.340-50_340-49insA	XP_011538921.1:n.340-50_340-49insA
XM_011540620.1:c.499-50_499-49insA	XP_011538922.1:n.499-50_499-49insA
NM_000085.5:c.499-50_499-49insA MANE Select	NP_000076.2:n.499-50_499-49insA