Canonical Allele Identifier: CA338641078

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16378004C>T (hg19) ; chr1:g.16051509C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16051509C>T , CM000663.2:g.16051509C>T	GRCh38
NC_000001.10:g.16378004C>T , CM000663.1:g.16378004C>T	GRCh37
NC_000001.9:g.16250591C>T	NCBI36
NG_013079.1:g.12758C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1259C>T	ENSP00000507062.1:p.Pro420Leu
ENST00000682793.1:c.1259C>T	ENSP00000506910.1:p.Pro420Leu
ENST00000682838.1:c.*1001C>T	ENSP00000507652.1:n.*1001C>T
ENST00000683578.1:c.1259C>T	ENSP00000507430.1:p.Pro420Leu
ENST00000683606.1:n.874C>T
ENST00000683661.1:n.2794C>T
ENST00000684324.1:c.1259C>T	ENSP00000507937.1:p.Pro420Leu
ENST00000684545.1:c.1259C>T	ENSP00000506733.1:p.Pro420Leu
ENST00000684624.1:n.636C>T
ENST00000684714.1:c.1259C>T	ENSP00000506861.1:p.Pro420Leu
ENST00000684731.1:n.720C>T
ENST00000375679.9:c.1259C>T MANE Select	ENSP00000364831.5:p.Pro420Leu
ENST00000375667.7:c.752C>T	ENSP00000364819.3:p.Pro251Leu
ENST00000375679.8:c.1259C>T	ENSP00000364831.4:p.Pro420Leu
ENST00000619181.4:c.878C>T	ENSP00000483866.1:p.Pro293Leu
NM_000085.4:c.1259C>T	NP_000076.2:p.Pro420Leu
NM_001165945.2:c.752C>T	NP_001159417.2:p.Pro251Leu
XM_011540619.1:c.1100C>T	XP_011538921.1:p.Pro367Leu
XM_011540620.1:c.1259C>T	XP_011538922.1:p.Pro420Leu
XM_011540621.1:c.608C>T	XP_011538923.1:p.Pro203Leu
NM_000085.5:c.1259C>T MANE Select	NP_000076.2:p.Pro420Leu