Canonical Allele Identifier: CA1140009923

Gene: CLCNKA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024618T= , CM000663.2:g.16024618T=	GRCh38
NC_000001.10:g.16351113T= , CM000663.1:g.16351113T=	GRCh37
NC_000001.9:g.16223700T=	NCBI36
NG_009359.1:g.7628T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.230-145T= MANE Select	ENSP00000332771.4:n.230-145T=
ENST00000331433.4:c.230-145T=	ENSP00000332771.4:n.230-145T=
ENST00000375692.5:c.230-145T=	ENSP00000364844.1:n.230-145T=
ENST00000439316.6:c.229+690T=	ENSP00000414445.2:n.229+690T=
ENST00000464764.5:n.889-241T=
ENST00000495784.1:n.388-145T=
NM_001042704.1:c.230-145T=	NP_001036169.1:n.230-145T=
NM_001257139.1:c.229+690T=	NP_001244068.1:n.229+690T=
NM_004070.3:c.230-145T=	NP_004061.3:n.230-145T=
NM_004070.4:c.230-145T= MANE Select	NP_004061.3:n.230-145T=
NM_001042704.2:c.230-145T=	NP_001036169.1:n.230-145T=
NM_001257139.2:c.229+690T=	NP_001244068.1:n.229+690T=