Canonical Allele Identifier: CA416249764

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16378227T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16051732T>C , CM000663.2:g.16051732T>C	GRCh38
NC_000001.10:g.16378227T>C , CM000663.1:g.16378227T>C	GRCh37
NC_000001.9:g.16250814T>C	NCBI36
NG_013079.1:g.12981T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.1320T>C	ENSP00000507062.1:p.Phe440=
ENST00000682793.1:c.1320T>C	ENSP00000506910.1:p.Phe440=
ENST00000682838.1:c.*1062T>C	ENSP00000507652.1:n.*1062T>C
ENST00000683578.1:c.1320T>C	ENSP00000507430.1:p.Phe440=
ENST00000683606.1:n.935T>C
ENST00000683661.1:n.2855T>C
ENST00000684324.1:c.1320T>C	ENSP00000507937.1:p.Phe440=
ENST00000684545.1:c.1320T>C	ENSP00000506733.1:p.Phe440=
ENST00000684624.1:n.697T>C
ENST00000684714.1:c.1320T>C	ENSP00000506861.1:p.Phe440=
ENST00000684731.1:n.781T>C
ENST00000375679.9:c.1320T>C MANE Select	ENSP00000364831.5:p.Phe440=
ENST00000375667.7:c.813T>C	ENSP00000364819.3:p.Phe271=
ENST00000375679.8:c.1320T>C	ENSP00000364831.4:p.Phe440=
ENST00000619181.4:c.939T>C	ENSP00000483866.1:p.Phe313=
NM_000085.4:c.1320T>C	NP_000076.2:p.Phe440=
NM_001165945.2:c.813T>C	NP_001159417.2:p.Phe271=
XM_011540619.1:c.1161T>C	XP_011538921.1:p.Phe387=
XM_011540620.1:c.1320T>C	XP_011538922.1:p.Phe440=
XM_011540621.1:c.669T>C	XP_011538923.1:p.Phe223=
NM_000085.5:c.1320T>C MANE Select	NP_000076.2:p.Phe440=