Canonical Allele Identifier: CA416227052

Gene: CLCNKA

Linked Data

• MyVariant Identifiers: chr1:g.16351319T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024824T>A , CM000663.2:g.16024824T>A	GRCh38
NC_000001.10:g.16351319T>A , CM000663.1:g.16351319T>A	GRCh37
NC_000001.9:g.16223906T>A	NCBI36
NG_009359.1:g.7834T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.291T>A MANE Select	ENSP00000332771.4:p.Thr97=
ENST00000331433.4:c.291T>A	ENSP00000332771.4:p.Thr97=
ENST00000375692.5:c.291T>A	ENSP00000364844.1:p.Thr97=
ENST00000439316.6:c.229+896T>A	ENSP00000414445.2:n.229+896T>A
ENST00000464764.5:n.889-35T>A
ENST00000495784.1:n.449T>A
NM_001042704.1:c.291T>A	NP_001036169.1:p.Thr97=
NM_001257139.1:c.229+896T>A	NP_001244068.1:n.229+896T>A
NM_004070.3:c.291T>A	NP_004061.3:p.Thr97=
NM_004070.4:c.291T>A MANE Select	NP_004061.3:p.Thr97=
NM_001042704.2:c.291T>A	NP_001036169.1:p.Thr97=
NM_001257139.2:c.229+896T>A	NP_001244068.1:n.229+896T>A