Canonical Allele Identifier: CA416256559

Gene: CLCNKB

Linked Data

• gnomAD v4: 1-16055478-G-C
• MyVariant Identifiers: chr1:g.16381973G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16055478G>C , CM000663.2:g.16055478G>C	GRCh38
NC_000001.10:g.16381973G>C , CM000663.1:g.16381973G>C	GRCh37
NC_000001.9:g.16254560G>C	NCBI36
NG_013079.1:g.16727G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1800G>C	ENSP00000507062.1:p.Val600=
ENST00000682793.1:c.1800G>C	ENSP00000506910.1:p.Val600=
ENST00000682838.1:c.*1542G>C	ENSP00000507652.1:n.*1542G>C
ENST00000683578.1:c.1800G>C	ENSP00000507430.1:p.Val600=
ENST00000683606.1:n.1406G>C
ENST00000683661.1:n.3335G>C
ENST00000684324.1:c.1800G>C	ENSP00000507937.1:p.Val600=
ENST00000684545.1:c.1800G>C	ENSP00000506733.1:p.Val600=
ENST00000684624.1:n.1177G>C
ENST00000684714.1:c.*20G>C	ENSP00000506861.1:n.*20G>C
ENST00000684731.1:n.1127G>C
ENST00000375679.9:c.1800G>C MANE Select	ENSP00000364831.5:p.Val600=
ENST00000375667.7:c.1293G>C	ENSP00000364819.3:p.Val431=
ENST00000375679.8:c.1800G>C	ENSP00000364831.4:p.Val600=
ENST00000431772.1:c.267G>C	ENSP00000389344.1:p.Val89=
ENST00000619181.4:c.1294-1709G>C	ENSP00000483866.1:n.1294-1709G>C
NM_000085.4:c.1800G>C	NP_000076.2:p.Val600=
NM_001165945.2:c.1293G>C	NP_001159417.2:p.Val431=
XM_011540619.1:c.1641G>C	XP_011538921.1:p.Val547=
XM_011540621.1:c.1149G>C	XP_011538923.1:p.Val383=
NM_000085.5:c.1800G>C MANE Select	NP_000076.2:p.Val600=