Canonical Allele Identifier: CA521294347

Gene: CLCNKA

Linked Data

• dbSNP Id: rs1197305464
• gnomAD v2: 1-16351499-G-A
• gnomAD v3: 1-16025004-G-A
• gnomAD v4: 1-16025004-G-A
• MyVariant Identifiers: chr1:g.16351499G>A (hg19) ; chr1:g.16025004G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16025004G>A , CM000663.2:g.16025004G>A	GRCh38
NC_000001.10:g.16351499G>A , CM000663.1:g.16351499G>A	GRCh37
NC_000001.9:g.16224086G>A	NCBI36
NG_009359.1:g.8014G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.358+113G>A MANE Select	ENSP00000332771.4:n.358+113G>A
ENST00000331433.4:c.358+113G>A	ENSP00000332771.4:n.358+113G>A
ENST00000375692.5:c.358+113G>A	ENSP00000364844.1:n.358+113G>A
ENST00000439316.6:c.229+1076G>A	ENSP00000414445.2:n.229+1076G>A
ENST00000464764.5:n.921+113G>A
ENST00000495784.1:n.516+113G>A
NM_001042704.1:c.358+113G>A	NP_001036169.1:n.358+113G>A
NM_001257139.1:c.229+1076G>A	NP_001244068.1:n.229+1076G>A
NM_004070.3:c.358+113G>A	NP_004061.3:n.358+113G>A
NM_004070.4:c.358+113G>A MANE Select	NP_004061.3:n.358+113G>A
NM_001042704.2:c.358+113G>A	NP_001036169.1:n.358+113G>A
NM_001257139.2:c.229+1076G>A	NP_001244068.1:n.229+1076G>A