Canonical Allele Identifier: CA890091177

Gene: CLCNKA

Linked Data

• dbSNP Id: rs1338425506
• MyVariant Identifiers: chr1:g.16351458G>C (hg19) ; chr1:g.16024963G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024963G>C , CM000663.2:g.16024963G>C	GRCh38
NC_000001.10:g.16351458G>C , CM000663.1:g.16351458G>C	GRCh37
NC_000001.9:g.16224045G>C	NCBI36
NG_009359.1:g.7973G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.358+72G>C MANE Select	ENSP00000332771.4:n.358+72G>C
ENST00000331433.4:c.358+72G>C	ENSP00000332771.4:n.358+72G>C
ENST00000375692.5:c.358+72G>C	ENSP00000364844.1:n.358+72G>C
ENST00000439316.6:c.229+1035G>C	ENSP00000414445.2:n.229+1035G>C
ENST00000464764.5:n.921+72G>C
ENST00000495784.1:n.516+72G>C
NM_001042704.1:c.358+72G>C	NP_001036169.1:n.358+72G>C
NM_001257139.1:c.229+1035G>C	NP_001244068.1:n.229+1035G>C
NM_004070.3:c.358+72G>C	NP_004061.3:n.358+72G>C
NM_004070.4:c.358+72G>C MANE Select	NP_004061.3:n.358+72G>C
NM_001042704.2:c.358+72G>C	NP_001036169.1:n.358+72G>C
NM_001257139.2:c.229+1035G>C	NP_001244068.1:n.229+1035G>C