Canonical Allele Identifier: CA2643559934

Gene: CLCNKA

Linked Data

• gnomAD v4: 1-16024626-G-GGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024627_16024628insAAG , CM000663.2:g.16024627_16024628insAAG	GRCh38
NC_000001.10:g.16351122_16351123insAAG , CM000663.1:g.16351122_16351123insAAG	GRCh37
NC_000001.9:g.16223709_16223710insAAG	NCBI36
NG_009359.1:g.7637_7638insAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.230-136_230-135insAAG MANE Select	ENSP00000332771.4:n.230-136_230-135insAAG
ENST00000331433.4:c.230-136_230-135insAAG	ENSP00000332771.4:n.230-136_230-135insAAG
ENST00000375692.5:c.230-136_230-135insAAG	ENSP00000364844.1:n.230-136_230-135insAAG
ENST00000439316.6:c.229+699_229+700insAAG	ENSP00000414445.2:n.229+699_229+700insAAG
ENST00000464764.5:n.889-232_889-231insAAG
ENST00000495784.1:n.388-136_388-135insAAG
NM_001042704.1:c.230-136_230-135insAAG	NP_001036169.1:n.230-136_230-135insAAG
NM_001257139.1:c.229+699_229+700insAAG	NP_001244068.1:n.229+699_229+700insAAG
NM_004070.3:c.230-136_230-135insAAG	NP_004061.3:n.230-136_230-135insAAG
NM_004070.4:c.230-136_230-135insAAG MANE Select	NP_004061.3:n.230-136_230-135insAAG
NM_001042704.2:c.230-136_230-135insAAG	NP_001036169.1:n.230-136_230-135insAAG
NM_001257139.2:c.229+699_229+700insAAG	NP_001244068.1:n.229+699_229+700insAAG