Canonical Allele Identifier: CA890090705

Gene: CLCNKB

Linked Data

• dbSNP Id: rs1335531233
• MyVariant Identifiers: chr1:g.16375287_16375289del (hg19) ; chr1:g.16048792_16048794del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16048794_16048796del , CM000663.2:g.16048794_16048796del	GRCh38
NC_000001.10:g.16375289_16375291del , CM000663.1:g.16375289_16375291del	GRCh37
NC_000001.9:g.16247876_16247878del	NCBI36
NG_013079.1:g.10043_10045del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682338.1:c.655+212_655+214del	ENSP00000507062.1:n.655+212_655+214del
ENST00000682793.1:c.655+212_655+214del	ENSP00000506910.1:n.655+212_655+214del
ENST00000682838.1:c.*313+212_*313+214del	ENSP00000507652.1:n.*313+212_*313+214del
ENST00000683578.1:c.655+212_655+214del	ENSP00000507430.1:n.655+212_655+214del
ENST00000683661.1:n.2190+212_2190+214del
ENST00000684324.1:c.655+212_655+214del	ENSP00000507937.1:n.655+212_655+214del
ENST00000684545.1:c.655+212_655+214del	ENSP00000506733.1:n.655+212_655+214del
ENST00000684714.1:c.655+212_655+214del	ENSP00000506861.1:n.655+212_655+214del
ENST00000684731.1:n.116+212_116+214del
ENST00000375679.9:c.655+212_655+214del MANE Select	ENSP00000364831.5:n.655+212_655+214del
ENST00000375667.7:c.-178_-176del	ENSP00000364819.3:n.-178_-176del
ENST00000375679.8:c.655+212_655+214del	ENSP00000364831.4:n.655+212_655+214del
ENST00000619181.4:c.587+280_587+282del	ENSP00000483866.1:n.587+280_587+282del
NM_000085.4:c.655+212_655+214del	NP_000076.2:n.655+212_655+214del
NM_001165945.2:c.-178_-176del	NP_001159417.2:n.-178_-176del
XM_011540619.1:c.496+212_496+214del	XP_011538921.1:n.496+212_496+214del
XM_011540620.1:c.655+212_655+214del	XP_011538922.1:n.655+212_655+214del
XM_011540621.1:c.-234_-232del	XP_011538923.1:n.-234_-232del
NM_000085.5:c.655+212_655+214del MANE Select	NP_000076.2:n.655+212_655+214del