Canonical Allele Identifier: CA890091195

Gene: CLCNKA

Linked Data

• dbSNP Id: rs1231602384
• gnomAD v3: 1-16024994-G-A
• gnomAD v4: 1-16024994-G-A
• MyVariant Identifiers: chr1:g.16351489G>A (hg19) ; chr1:g.16024994G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024994G>A , CM000663.2:g.16024994G>A	GRCh38
NC_000001.10:g.16351489G>A , CM000663.1:g.16351489G>A	GRCh37
NC_000001.9:g.16224076G>A	NCBI36
NG_009359.1:g.8004G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.358+103G>A MANE Select	ENSP00000332771.4:n.358+103G>A
ENST00000331433.4:c.358+103G>A	ENSP00000332771.4:n.358+103G>A
ENST00000375692.5:c.358+103G>A	ENSP00000364844.1:n.358+103G>A
ENST00000439316.6:c.229+1066G>A	ENSP00000414445.2:n.229+1066G>A
ENST00000464764.5:n.921+103G>A
ENST00000495784.1:n.516+103G>A
NM_001042704.1:c.358+103G>A	NP_001036169.1:n.358+103G>A
NM_001257139.1:c.229+1066G>A	NP_001244068.1:n.229+1066G>A
NM_004070.3:c.358+103G>A	NP_004061.3:n.358+103G>A
NM_004070.4:c.358+103G>A MANE Select	NP_004061.3:n.358+103G>A
NM_001042704.2:c.358+103G>A	NP_001036169.1:n.358+103G>A
NM_001257139.2:c.229+1066G>A	NP_001244068.1:n.229+1066G>A