Canonical Allele Identifier: CA2643559941

Gene: CLCNKA

Linked Data

• gnomAD v4: 1-16024629-T-TACTC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024629_16024630insACTC , CM000663.2:g.16024629_16024630insACTC	GRCh38
NC_000001.10:g.16351124_16351125insACTC , CM000663.1:g.16351124_16351125insACTC	GRCh37
NC_000001.9:g.16223711_16223712insACTC	NCBI36
NG_009359.1:g.7639_7640insACTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.230-134_230-133insACTC MANE Select	ENSP00000332771.4:n.230-134_230-133insACTC
ENST00000331433.4:c.230-134_230-133insACTC	ENSP00000332771.4:n.230-134_230-133insACTC
ENST00000375692.5:c.230-134_230-133insACTC	ENSP00000364844.1:n.230-134_230-133insACTC
ENST00000439316.6:c.229+701_229+702insACTC	ENSP00000414445.2:n.229+701_229+702insACTC
ENST00000464764.5:n.889-230_889-229insACTC
ENST00000495784.1:n.388-134_388-133insACTC
NM_001042704.1:c.230-134_230-133insACTC	NP_001036169.1:n.230-134_230-133insACTC
NM_001257139.1:c.229+701_229+702insACTC	NP_001244068.1:n.229+701_229+702insACTC
NM_004070.3:c.230-134_230-133insACTC	NP_004061.3:n.230-134_230-133insACTC
NM_004070.4:c.230-134_230-133insACTC MANE Select	NP_004061.3:n.230-134_230-133insACTC
NM_001042704.2:c.230-134_230-133insACTC	NP_001036169.1:n.230-134_230-133insACTC
NM_001257139.2:c.229+701_229+702insACTC	NP_001244068.1:n.229+701_229+702insACTC