Canonical Allele Identifier: CA890090841

Gene: CLCNKA

Linked Data

• dbSNP Id: rs4083858
• MyVariant Identifiers: chr1:g.16351113T>A (hg19) ; chr1:g.16024618T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024618T>A , CM000663.2:g.16024618T>A	GRCh38
NC_000001.10:g.16351113T>A , CM000663.1:g.16351113T>A	GRCh37
NC_000001.9:g.16223700T>A	NCBI36
NG_009359.1:g.7628T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.230-145T>A MANE Select	ENSP00000332771.4:n.230-145T>A
ENST00000331433.4:c.230-145T>A	ENSP00000332771.4:n.230-145T>A
ENST00000375692.5:c.230-145T>A	ENSP00000364844.1:n.230-145T>A
ENST00000439316.6:c.229+690T>A	ENSP00000414445.2:n.229+690T>A
ENST00000464764.5:n.889-241T>A
ENST00000495784.1:n.388-145T>A
NM_001042704.1:c.230-145T>A	NP_001036169.1:n.230-145T>A
NM_001257139.1:c.229+690T>A	NP_001244068.1:n.229+690T>A
NM_004070.3:c.230-145T>A	NP_004061.3:n.230-145T>A
NM_004070.4:c.230-145T>A MANE Select	NP_004061.3:n.230-145T>A
NM_001042704.2:c.230-145T>A	NP_001036169.1:n.230-145T>A
NM_001257139.2:c.229+690T>A	NP_001244068.1:n.229+690T>A