Canonical Allele Identifier: CA1155626881

Gene: CLCNKA

Linked Data

• dbSNP Id: rs1570297471
• gnomAD v4: 1-16025019-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16025019T>C , CM000663.2:g.16025019T>C	GRCh38
NC_000001.10:g.16351514T>C , CM000663.1:g.16351514T>C	GRCh37
NC_000001.9:g.16224101T>C	NCBI36
NG_009359.1:g.8029T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.358+128T>C MANE Select	ENSP00000332771.4:n.358+128T>C
ENST00000331433.4:c.358+128T>C	ENSP00000332771.4:n.358+128T>C
ENST00000375692.5:c.358+128T>C	ENSP00000364844.1:n.358+128T>C
ENST00000439316.6:c.230-1089T>C	ENSP00000414445.2:n.230-1089T>C
ENST00000464764.5:n.921+128T>C
ENST00000495784.1:n.516+128T>C
NM_001042704.1:c.358+128T>C	NP_001036169.1:n.358+128T>C
NM_001257139.1:c.230-1089T>C	NP_001244068.1:n.230-1089T>C
NM_004070.3:c.358+128T>C	NP_004061.3:n.358+128T>C
NM_004070.4:c.358+128T>C MANE Select	NP_004061.3:n.358+128T>C
NM_001042704.2:c.358+128T>C	NP_001036169.1:n.358+128T>C
NM_001257139.2:c.230-1089T>C	NP_001244068.1:n.230-1089T>C