Canonical Allele Identifier: CA18309198

Gene: CLCNKA

Linked Data

• dbSNP Id: rs905736776
• gnomAD v3: 1-16024593-T-C
• gnomAD v4: 1-16024593-T-C
• MyVariant Identifiers: chr1:g.16351088T>C (hg19) ; chr1:g.16024593T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024593T>C , CM000663.2:g.16024593T>C	GRCh38
NC_000001.10:g.16351088T>C , CM000663.1:g.16351088T>C	GRCh37
NC_000001.9:g.16223675T>C	NCBI36
NG_009359.1:g.7603T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.230-170T>C MANE Select	ENSP00000332771.4:n.230-170T>C
ENST00000331433.4:c.230-170T>C	ENSP00000332771.4:n.230-170T>C
ENST00000375692.5:c.230-170T>C	ENSP00000364844.1:n.230-170T>C
ENST00000439316.6:c.229+665T>C	ENSP00000414445.2:n.229+665T>C
ENST00000464764.5:n.889-266T>C
ENST00000495784.1:n.388-170T>C
NM_001042704.1:c.230-170T>C	NP_001036169.1:n.230-170T>C
NM_001257139.1:c.229+665T>C	NP_001244068.1:n.229+665T>C
NM_004070.3:c.230-170T>C	NP_004061.3:n.230-170T>C
NM_004070.4:c.230-170T>C MANE Select	NP_004061.3:n.230-170T>C
NM_001042704.2:c.230-170T>C	NP_001036169.1:n.230-170T>C
NM_001257139.2:c.229+665T>C	NP_001244068.1:n.229+665T>C