Canonical Allele Identifier: CA338644743

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16381969T>C (hg19) ; chr1:g.16055474T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16055474T>C , CM000663.2:g.16055474T>C	GRCh38
NC_000001.10:g.16381969T>C , CM000663.1:g.16381969T>C	GRCh37
NC_000001.9:g.16254556T>C	NCBI36
NG_013079.1:g.16723T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1796T>C	ENSP00000507062.1:p.Leu599Pro
ENST00000682793.1:c.1796T>C	ENSP00000506910.1:p.Leu599Pro
ENST00000682838.1:c.*1538T>C	ENSP00000507652.1:n.*1538T>C
ENST00000683578.1:c.1796T>C	ENSP00000507430.1:p.Leu599Pro
ENST00000683606.1:n.1402T>C
ENST00000683661.1:n.3331T>C
ENST00000684324.1:c.1796T>C	ENSP00000507937.1:p.Leu599Pro
ENST00000684545.1:c.1796T>C	ENSP00000506733.1:p.Leu599Pro
ENST00000684624.1:n.1173T>C
ENST00000684714.1:c.*16T>C	ENSP00000506861.1:n.*16T>C
ENST00000684731.1:n.1123T>C
ENST00000375679.9:c.1796T>C MANE Select	ENSP00000364831.5:p.Leu599Pro
ENST00000375667.7:c.1289T>C	ENSP00000364819.3:p.Leu430Pro
ENST00000375679.8:c.1796T>C	ENSP00000364831.4:p.Leu599Pro
ENST00000431772.1:c.263T>C	ENSP00000389344.1:p.Leu88Pro
ENST00000619181.4:c.1294-1713T>C	ENSP00000483866.1:n.1294-1713T>C
NM_000085.4:c.1796T>C	NP_000076.2:p.Leu599Pro
NM_001165945.2:c.1289T>C	NP_001159417.2:p.Leu430Pro
XM_011540619.1:c.1637T>C	XP_011538921.1:p.Leu546Pro
XM_011540621.1:c.1145T>C	XP_011538923.1:p.Leu382Pro
NM_000085.5:c.1796T>C MANE Select	NP_000076.2:p.Leu599Pro