Canonical Allele Identifier: CA416240555

Gene: CLCNKB

Linked Data

• gnomAD v4: 1-16048548-G-A
• MyVariant Identifiers: chr1:g.16375043G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16048548G>A , CM000663.2:g.16048548G>A	GRCh38
NC_000001.10:g.16375043G>A , CM000663.1:g.16375043G>A	GRCh37
NC_000001.9:g.16247630G>A	NCBI36
NG_013079.1:g.9797G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682338.1:c.621G>A	ENSP00000507062.1:p.Val207=
ENST00000682793.1:c.621G>A	ENSP00000506910.1:p.Val207=
ENST00000682838.1:c.*279G>A	ENSP00000507652.1:n.*279G>A
ENST00000683578.1:c.621G>A	ENSP00000507430.1:p.Val207=
ENST00000683661.1:n.2156G>A
ENST00000684324.1:c.621G>A	ENSP00000507937.1:p.Val207=
ENST00000684545.1:c.621G>A	ENSP00000506733.1:p.Val207=
ENST00000684714.1:c.621G>A	ENSP00000506861.1:p.Val207=
ENST00000684731.1:n.82G>A
ENST00000375679.9:c.621G>A MANE Select	ENSP00000364831.5:p.Val207=
ENST00000375679.8:c.621G>A	ENSP00000364831.4:p.Val207=
ENST00000619181.4:c.587+34G>A	ENSP00000483866.1:n.587+34G>A
NM_000085.4:c.621G>A	NP_000076.2:p.Val207=
XM_011540619.1:c.462G>A	XP_011538921.1:p.Val154=
XM_011540620.1:c.621G>A	XP_011538922.1:p.Val207=
NM_000085.5:c.621G>A MANE Select	NP_000076.2:p.Val207=