Canonical Allele Identifier: CA1155655512

Gene: CLCNKB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16048545_16048546delinsAG , CM000663.2:g.16048545_16048546delinsAG	GRCh38
NC_000001.10:g.16375040_16375041delinsAG , CM000663.1:g.16375040_16375041delinsAG	GRCh37
NC_000001.9:g.16247627_16247628delinsAG	NCBI36
NG_013079.1:g.9794_9795delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000682338.1:c.618_619delinsAG	ENSP00000507062.1:p.Ala206=
ENST00000682793.1:c.618_619delinsAG	ENSP00000506910.1:p.Ala206=
ENST00000682838.1:c.*276_*277delinsAG	ENSP00000507652.1:n.*276_*277delinsAG
ENST00000683578.1:c.618_619delinsAG	ENSP00000507430.1:p.Ala206=
ENST00000683661.1:n.2153_2154delinsAG
ENST00000684324.1:c.618_619delinsAG	ENSP00000507937.1:p.Ala206=
ENST00000684545.1:c.618_619delinsAG	ENSP00000506733.1:p.Ala206=
ENST00000684714.1:c.618_619delinsAG	ENSP00000506861.1:p.Ala206=
ENST00000684731.1:n.79_80delinsAG
ENST00000375679.9:c.618_619delinsAG MANE Select	ENSP00000364831.5:p.Ala206=
ENST00000375679.8:c.618_619delinsAG	ENSP00000364831.4:p.Ala206=
ENST00000619181.4:c.587+31_587+32delinsAG	ENSP00000483866.1:n.587+31_587+32delinsAG...
NM_000085.4:c.618_619delinsAG	NP_000076.2:p.Ala206=
XM_011540619.1:c.459_460delinsAG	XP_011538921.1:p.Ala153=
XM_011540620.1:c.618_619delinsAG	XP_011538922.1:p.Ala206=
NM_000085.5:c.618_619delinsAG MANE Select	NP_000076.2:p.Ala206=