Canonical Allele Identifier: CA338635329

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16375038G>C (hg19) ; chr1:g.16048543G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16048543G>C , CM000663.2:g.16048543G>C	GRCh38
NC_000001.10:g.16375038G>C , CM000663.1:g.16375038G>C	GRCh37
NC_000001.9:g.16247625G>C	NCBI36
NG_013079.1:g.9792G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682338.1:c.616G>C	ENSP00000507062.1:p.Ala206Pro
ENST00000682793.1:c.616G>C	ENSP00000506910.1:p.Ala206Pro
ENST00000682838.1:c.*274G>C	ENSP00000507652.1:n.*274G>C
ENST00000683578.1:c.616G>C	ENSP00000507430.1:p.Ala206Pro
ENST00000683661.1:n.2151G>C
ENST00000684324.1:c.616G>C	ENSP00000507937.1:p.Ala206Pro
ENST00000684545.1:c.616G>C	ENSP00000506733.1:p.Ala206Pro
ENST00000684714.1:c.616G>C	ENSP00000506861.1:p.Ala206Pro
ENST00000684731.1:n.77G>C
ENST00000375679.9:c.616G>C MANE Select	ENSP00000364831.5:p.Ala206Pro
ENST00000375679.8:c.616G>C	ENSP00000364831.4:p.Ala206Pro
ENST00000619181.4:c.587+29G>C	ENSP00000483866.1:n.587+29G>C
NM_000085.4:c.616G>C	NP_000076.2:p.Ala206Pro
XM_011540619.1:c.457G>C	XP_011538921.1:p.Ala153Pro
XM_011540620.1:c.616G>C	XP_011538922.1:p.Ala206Pro
NM_000085.5:c.616G>C MANE Select	NP_000076.2:p.Ala206Pro