Canonical Allele Identifier: CA1146971109

Gene: CLCNKA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024779C= , CM000663.2:g.16024779C=	GRCh38
NC_000001.10:g.16351274C= , CM000663.1:g.16351274C=	GRCh37
NC_000001.9:g.16223861C=	NCBI36
NG_009359.1:g.7789C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000331433.5:c.246C= MANE Select	ENSP00000332771.4:p.Tyr82=
ENST00000331433.4:c.246C=	ENSP00000332771.4:p.Tyr82=
ENST00000375692.5:c.246C=	ENSP00000364844.1:p.Tyr82=
ENST00000439316.6:c.229+851C=	ENSP00000414445.2:n.229+851C=
ENST00000464764.5:n.889-80C=
ENST00000495784.1:n.404C=
NM_001042704.1:c.246C=	NP_001036169.1:p.Tyr82=
NM_001257139.1:c.229+851C=	NP_001244068.1:n.229+851C=
NM_004070.3:c.246C=	NP_004061.3:p.Tyr82=
NM_004070.4:c.246C= MANE Select	NP_004061.3:p.Tyr82=
NM_001042704.2:c.246C=	NP_001036169.1:p.Tyr82=
NM_001257139.2:c.229+851C=	NP_001244068.1:n.229+851C=