Canonical Allele Identifier: CA338609742
Gene: CLCNKA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16024838C>A , CM000663.2:g.16024838C>A GRCh38
NC_000001.10:g.16351333C>A , CM000663.1:g.16351333C>A GRCh37
NC_000001.9:g.16223920C>A NCBI36
NG_009359.1:g.7848C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331433.5:c.305C>A MANE Select ENSP00000332771.4:p.Ala102Asp
ENST00000331433.4:c.305C>A ENSP00000332771.4:p.Ala102Asp
ENST00000375692.5:c.305C>A ENSP00000364844.1:p.Ala102Asp
ENST00000439316.6:c.229+910C>A ENSP00000414445.2:n.229+910C>A
ENST00000464764.5:n.889-21C>A
ENST00000495784.1:n.463C>A
NM_001042704.1:c.305C>A NP_001036169.1:p.Ala102Asp
NM_001257139.1:c.229+910C>A NP_001244068.1:n.229+910C>A
NM_004070.3:c.305C>A NP_004061.3:p.Ala102Asp
NM_004070.4:c.305C>A MANE Select NP_004061.3:p.Ala102Asp
NM_001042704.2:c.305C>A NP_001036169.1:p.Ala102Asp
NM_001257139.2:c.229+910C>A NP_001244068.1:n.229+910C>A