Canonical Allele Identifier: CA1155626805

Gene: CLCNKA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024968_16024969delinsCG , CM000663.2:g.16024968_16024969delinsCG	GRCh38
NC_000001.10:g.16351463_16351464delinsCG , CM000663.1:g.16351463_16351464delinsCG	GRCh37
NC_000001.9:g.16224050_16224051delinsCG	NCBI36
NG_009359.1:g.7978_7979delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.358+77_358+78delinsCG MANE Select	ENSP00000332771.4:n.358+77_358+78delinsCG
ENST00000331433.4:c.358+77_358+78delinsCG	ENSP00000332771.4:n.358+77_358+78delinsCG
ENST00000375692.5:c.358+77_358+78delinsCG	ENSP00000364844.1:n.358+77_358+78delinsCG
ENST00000439316.6:c.229+1040_229+1041delinsCG	ENSP00000414445.2:n.229+1040_229+1041delinsCG
ENST00000464764.5:n.921+77_921+78delinsCG
ENST00000495784.1:n.516+77_516+78delinsCG
NM_001042704.1:c.358+77_358+78delinsCG	NP_001036169.1:n.358+77_358+78delinsCG
NM_001257139.1:c.229+1040_229+1041delinsCG	NP_001244068.1:n.229+1040_229+1041delinsCG
NM_004070.3:c.358+77_358+78delinsCG	NP_004061.3:n.358+77_358+78delinsCG
NM_004070.4:c.358+77_358+78delinsCG MANE Select	NP_004061.3:n.358+77_358+78delinsCG
NM_001042704.2:c.358+77_358+78delinsCG	NP_001036169.1:n.358+77_358+78delinsCG
NM_001257139.2:c.229+1040_229+1041delinsCG	NP_001244068.1:n.229+1040_229+1041delinsCG