Canonical Allele Identifier: CA1155626115
Gene: CLCNKA HGNC NCBI

Linked Data

dbSNP Id: rs2022277428

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16024740C>G , CM000663.2:g.16024740C>G GRCh38
NC_000001.10:g.16351235C>G , CM000663.1:g.16351235C>G GRCh37
NC_000001.9:g.16223822C>G NCBI36
NG_009359.1:g.7750C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331433.5:c.230-23C>G MANE Select ENSP00000332771.4:n.230-23C>G
ENST00000331433.4:c.230-23C>G ENSP00000332771.4:n.230-23C>G
ENST00000375692.5:c.230-23C>G ENSP00000364844.1:n.230-23C>G
ENST00000439316.6:c.229+812C>G ENSP00000414445.2:n.229+812C>G
ENST00000464764.5:n.889-119C>G
ENST00000495784.1:n.388-23C>G
NM_001042704.1:c.230-23C>G NP_001036169.1:n.230-23C>G
NM_001257139.1:c.229+812C>G NP_001244068.1:n.229+812C>G
NM_004070.3:c.230-23C>G NP_004061.3:n.230-23C>G
NM_004070.4:c.230-23C>G MANE Select NP_004061.3:n.230-23C>G
NM_001042704.2:c.230-23C>G NP_001036169.1:n.230-23C>G
NM_001257139.2:c.229+812C>G NP_001244068.1:n.229+812C>G