Canonical Allele Identifier: CA2643560063
Gene: CLCNKA HGNC NCBI

Linked Data

gnomAD v4: 1-16024705-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16024705T>A , CM000663.2:g.16024705T>A GRCh38
NC_000001.10:g.16351200T>A , CM000663.1:g.16351200T>A GRCh37
NC_000001.9:g.16223787T>A NCBI36
NG_009359.1:g.7715T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000331433.5:c.230-58T>A MANE Select ENSP00000332771.4:n.230-58T>A
ENST00000331433.4:c.230-58T>A ENSP00000332771.4:n.230-58T>A
ENST00000375692.5:c.230-58T>A ENSP00000364844.1:n.230-58T>A
ENST00000439316.6:c.229+777T>A ENSP00000414445.2:n.229+777T>A
ENST00000464764.5:n.889-154T>A
ENST00000495784.1:n.388-58T>A
NM_001042704.1:c.230-58T>A NP_001036169.1:n.230-58T>A
NM_001257139.1:c.229+777T>A NP_001244068.1:n.229+777T>A
NM_004070.3:c.230-58T>A NP_004061.3:n.230-58T>A
NM_004070.4:c.230-58T>A MANE Select NP_004061.3:n.230-58T>A
NM_001042704.2:c.230-58T>A NP_001036169.1:n.230-58T>A
NM_001257139.2:c.229+777T>A NP_001244068.1:n.229+777T>A