Canonical Allele Identifier: CA338644801

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16381978C>T (hg19) ; chr1:g.16055483C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16055483C>T , CM000663.2:g.16055483C>T	GRCh38
NC_000001.10:g.16381978C>T , CM000663.1:g.16381978C>T	GRCh37
NC_000001.9:g.16254565C>T	NCBI36
NG_013079.1:g.16732C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1805C>T	ENSP00000507062.1:p.Ala602Val
ENST00000682793.1:c.1805C>T	ENSP00000506910.1:p.Ala602Val
ENST00000682838.1:c.*1547C>T	ENSP00000507652.1:n.*1547C>T
ENST00000683578.1:c.1805C>T	ENSP00000507430.1:p.Ala602Val
ENST00000683606.1:n.1411C>T
ENST00000683661.1:n.3340C>T
ENST00000684324.1:c.1805C>T	ENSP00000507937.1:p.Ala602Val
ENST00000684545.1:c.1805C>T	ENSP00000506733.1:p.Ala602Val
ENST00000684624.1:n.1182C>T
ENST00000684714.1:c.*25C>T	ENSP00000506861.1:n.*25C>T
ENST00000684731.1:n.1132C>T
ENST00000375679.9:c.1805C>T MANE Select	ENSP00000364831.5:p.Ala602Val
ENST00000375667.7:c.1298C>T	ENSP00000364819.3:p.Ala433Val
ENST00000375679.8:c.1805C>T	ENSP00000364831.4:p.Ala602Val
ENST00000431772.1:c.272C>T	ENSP00000389344.1:p.Ala91Val
ENST00000619181.4:c.1294-1704C>T	ENSP00000483866.1:n.1294-1704C>T
NM_000085.4:c.1805C>T	NP_000076.2:p.Ala602Val
NM_001165945.2:c.1298C>T	NP_001159417.2:p.Ala433Val
XM_011540619.1:c.1646C>T	XP_011538921.1:p.Ala549Val
XM_011540621.1:c.1154C>T	XP_011538923.1:p.Ala385Val
NM_000085.5:c.1805C>T MANE Select	NP_000076.2:p.Ala602Val