Canonical Allele Identifier: CA1155626751

Gene: CLCNKA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024941T= , CM000663.2:g.16024941T=	GRCh38
NC_000001.10:g.16351436T= , CM000663.1:g.16351436T=	GRCh37
NC_000001.9:g.16224023T=	NCBI36
NG_009359.1:g.7951T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.358+50T= MANE Select	ENSP00000332771.4:n.358+50T=
ENST00000331433.4:c.358+50T=	ENSP00000332771.4:n.358+50T=
ENST00000375692.5:c.358+50T=	ENSP00000364844.1:n.358+50T=
ENST00000439316.6:c.229+1013T=	ENSP00000414445.2:n.229+1013T=
ENST00000464764.5:n.921+50T=
ENST00000495784.1:n.516+50T=
NM_001042704.1:c.358+50T=	NP_001036169.1:n.358+50T=
NM_001257139.1:c.229+1013T=	NP_001244068.1:n.229+1013T=
NM_004070.3:c.358+50T=	NP_004061.3:n.358+50T=
NM_004070.4:c.358+50T= MANE Select	NP_004061.3:n.358+50T=
NM_001042704.2:c.358+50T=	NP_001036169.1:n.358+50T=
NM_001257139.2:c.229+1013T=	NP_001244068.1:n.229+1013T=