Canonical Allele Identifier: CA338644674

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16381950A>C (hg19) ; chr1:g.16055455A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16055455A>C , CM000663.2:g.16055455A>C	GRCh38
NC_000001.10:g.16381950A>C , CM000663.1:g.16381950A>C	GRCh37
NC_000001.9:g.16254537A>C	NCBI36
NG_013079.1:g.16704A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1777A>C	ENSP00000507062.1:p.Ile593Leu
ENST00000682793.1:c.1777A>C	ENSP00000506910.1:p.Ile593Leu
ENST00000682838.1:c.*1519A>C	ENSP00000507652.1:n.*1519A>C
ENST00000683578.1:c.1777A>C	ENSP00000507430.1:p.Ile593Leu
ENST00000683606.1:n.1383A>C
ENST00000683661.1:n.3312A>C
ENST00000684324.1:c.1777A>C	ENSP00000507937.1:p.Ile593Leu
ENST00000684545.1:c.1777A>C	ENSP00000506733.1:p.Ile593Leu
ENST00000684624.1:n.1154A>C
ENST00000684714.1:c.1728A>C	ENSP00000506861.1:p.Ala576=
ENST00000684731.1:n.1104A>C
ENST00000375679.9:c.1777A>C MANE Select	ENSP00000364831.5:p.Ile593Leu
ENST00000375667.7:c.1270A>C	ENSP00000364819.3:p.Ile424Leu
ENST00000375679.8:c.1777A>C	ENSP00000364831.4:p.Ile593Leu
ENST00000431772.1:c.244A>C	ENSP00000389344.1:p.Ile82Leu
ENST00000619181.4:c.1294-1732A>C	ENSP00000483866.1:n.1294-1732A>C
NM_000085.4:c.1777A>C	NP_000076.2:p.Ile593Leu
NM_001165945.2:c.1270A>C	NP_001159417.2:p.Ile424Leu
XM_011540619.1:c.1618A>C	XP_011538921.1:p.Ile540Leu
XM_011540621.1:c.1126A>C	XP_011538923.1:p.Ile376Leu
NM_000085.5:c.1777A>C MANE Select	NP_000076.2:p.Ile593Leu