Canonical Allele Identifier: CA1155626709

Gene: CLCNKA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024926_16024927delinsCA , CM000663.2:g.16024926_16024927delinsCA	GRCh38
NC_000001.10:g.16351421_16351422delinsCA , CM000663.1:g.16351421_16351422delinsCA	GRCh37
NC_000001.9:g.16224008_16224009delinsCA	NCBI36
NG_009359.1:g.7936_7937delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.358+35_358+36delinsCA MANE Select	ENSP00000332771.4:n.358+35_358+36delinsCA
ENST00000331433.4:c.358+35_358+36delinsCA	ENSP00000332771.4:n.358+35_358+36delinsCA
ENST00000375692.5:c.358+35_358+36delinsCA	ENSP00000364844.1:n.358+35_358+36delinsCA
ENST00000439316.6:c.229+998_229+999delinsCA	ENSP00000414445.2:n.229+998_229+999delinsCA
ENST00000464764.5:n.921+35_921+36delinsCA
ENST00000495784.1:n.516+35_516+36delinsCA
NM_001042704.1:c.358+35_358+36delinsCA	NP_001036169.1:n.358+35_358+36delinsCA
NM_001257139.1:c.229+998_229+999delinsCA	NP_001244068.1:n.229+998_229+999delinsCA
NM_004070.3:c.358+35_358+36delinsCA	NP_004061.3:n.358+35_358+36delinsCA
NM_004070.4:c.358+35_358+36delinsCA MANE Select	NP_004061.3:n.358+35_358+36delinsCA
NM_001042704.2:c.358+35_358+36delinsCA	NP_001036169.1:n.358+35_358+36delinsCA
NM_001257139.2:c.229+998_229+999delinsCA	NP_001244068.1:n.229+998_229+999delinsCA