Canonical Allele Identifier: CA1155626877

Gene: CLCNKA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16025016G= , CM000663.2:g.16025016G=	GRCh38
NC_000001.10:g.16351511G= , CM000663.1:g.16351511G=	GRCh37
NC_000001.9:g.16224098G=	NCBI36
NG_009359.1:g.8026G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.358+125G= MANE Select	ENSP00000332771.4:n.358+125G=
ENST00000331433.4:c.358+125G=	ENSP00000332771.4:n.358+125G=
ENST00000375692.5:c.358+125G=	ENSP00000364844.1:n.358+125G=
ENST00000439316.6:c.229+1088G=	ENSP00000414445.2:n.229+1088G=
ENST00000464764.5:n.921+125G=
ENST00000495784.1:n.516+125G=
NM_001042704.1:c.358+125G=	NP_001036169.1:n.358+125G=
NM_001257139.1:c.229+1088G=	NP_001244068.1:n.229+1088G=
NM_004070.3:c.358+125G=	NP_004061.3:n.358+125G=
NM_004070.4:c.358+125G= MANE Select	NP_004061.3:n.358+125G=
NM_001042704.2:c.358+125G=	NP_001036169.1:n.358+125G=
NM_001257139.2:c.229+1088G=	NP_001244068.1:n.229+1088G=