Canonical Allele Identifier: CA338635002

Gene: CLCNKB

Linked Data

• MyVariant Identifiers: chr1:g.16374898A>G (hg19) ; chr1:g.16048403A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16048403A>G , CM000663.2:g.16048403A>G	GRCh38
NC_000001.10:g.16374898A>G , CM000663.1:g.16374898A>G	GRCh37
NC_000001.9:g.16247485A>G	NCBI36
NG_013079.1:g.9652A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.559A>G	ENSP00000507062.1:p.Thr187Ala
ENST00000682793.1:c.559A>G	ENSP00000506910.1:p.Thr187Ala
ENST00000682838.1:c.*217A>G	ENSP00000507652.1:n.*217A>G
ENST00000683578.1:c.559A>G	ENSP00000507430.1:p.Thr187Ala
ENST00000683661.1:n.2094A>G
ENST00000684324.1:c.559A>G	ENSP00000507937.1:p.Thr187Ala
ENST00000684545.1:c.559A>G	ENSP00000506733.1:p.Thr187Ala
ENST00000684714.1:c.559A>G	ENSP00000506861.1:p.Thr187Ala
ENST00000684731.1:n.20A>G
ENST00000375679.9:c.559A>G MANE Select	ENSP00000364831.5:p.Thr187Ala
ENST00000375679.8:c.559A>G	ENSP00000364831.4:p.Thr187Ala
ENST00000619181.4:c.559A>G	ENSP00000483866.1:p.Thr187Ala
NM_000085.4:c.559A>G	NP_000076.2:p.Thr187Ala
XM_011540619.1:c.400A>G	XP_011538921.1:p.Thr134Ala
XM_011540620.1:c.559A>G	XP_011538922.1:p.Thr187Ala
NM_000085.5:c.559A>G MANE Select	NP_000076.2:p.Thr187Ala