Canonical Allele Identifier: CA1155626258

Gene: CLCNKA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024788T= , CM000663.2:g.16024788T=	GRCh38
NC_000001.10:g.16351283T= , CM000663.1:g.16351283T=	GRCh37
NC_000001.9:g.16223870T=	NCBI36
NG_009359.1:g.7798T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.255T= MANE Select	ENSP00000332771.4:p.Ile85=
ENST00000331433.4:c.255T=	ENSP00000332771.4:p.Ile85=
ENST00000375692.5:c.255T=	ENSP00000364844.1:p.Ile85=
ENST00000439316.6:c.229+860T=	ENSP00000414445.2:n.229+860T=
ENST00000464764.5:n.889-71T=
ENST00000495784.1:n.413T=
NM_001042704.1:c.255T=	NP_001036169.1:p.Ile85=
NM_001257139.1:c.229+860T=	NP_001244068.1:n.229+860T=
NM_004070.3:c.255T=	NP_004061.3:p.Ile85=
NM_004070.4:c.255T= MANE Select	NP_004061.3:p.Ile85=
NM_001042704.2:c.255T=	NP_001036169.1:p.Ile85=
NM_001257139.2:c.229+860T=	NP_001244068.1:n.229+860T=