Canonical Allele Identifier: CA416227139

Gene: CLCNKA

Linked Data

• MyVariant Identifiers: chr1:g.16351340C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024845C>A , CM000663.2:g.16024845C>A	GRCh38
NC_000001.10:g.16351340C>A , CM000663.1:g.16351340C>A	GRCh37
NC_000001.9:g.16223927C>A	NCBI36
NG_009359.1:g.7855C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.312C>A MANE Select	ENSP00000332771.4:p.Val104=
ENST00000331433.4:c.312C>A	ENSP00000332771.4:p.Val104=
ENST00000375692.5:c.312C>A	ENSP00000364844.1:p.Val104=
ENST00000439316.6:c.229+917C>A	ENSP00000414445.2:n.229+917C>A
ENST00000464764.5:n.889-14C>A
ENST00000495784.1:n.470C>A
NM_001042704.1:c.312C>A	NP_001036169.1:p.Val104=
NM_001257139.1:c.229+917C>A	NP_001244068.1:n.229+917C>A
NM_004070.3:c.312C>A	NP_004061.3:p.Val104=
NM_004070.4:c.312C>A MANE Select	NP_004061.3:p.Val104=
NM_001042704.2:c.312C>A	NP_001036169.1:p.Val104=
NM_001257139.2:c.229+917C>A	NP_001244068.1:n.229+917C>A