Canonical Allele Identifier: CA338609767

Gene: CLCNKA

Linked Data

• MyVariant Identifiers: chr1:g.16351339T>A (hg19) ; chr1:g.16024844T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024844T>A , CM000663.2:g.16024844T>A	GRCh38
NC_000001.10:g.16351339T>A , CM000663.1:g.16351339T>A	GRCh37
NC_000001.9:g.16223926T>A	NCBI36
NG_009359.1:g.7854T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.311T>A MANE Select	ENSP00000332771.4:p.Val104Asp
ENST00000331433.4:c.311T>A	ENSP00000332771.4:p.Val104Asp
ENST00000375692.5:c.311T>A	ENSP00000364844.1:p.Val104Asp
ENST00000439316.6:c.229+916T>A	ENSP00000414445.2:n.229+916T>A
ENST00000464764.5:n.889-15T>A
ENST00000495784.1:n.469T>A
NM_001042704.1:c.311T>A	NP_001036169.1:p.Val104Asp
NM_001257139.1:c.229+916T>A	NP_001244068.1:n.229+916T>A
NM_004070.3:c.311T>A	NP_004061.3:p.Val104Asp
NM_004070.4:c.311T>A MANE Select	NP_004061.3:p.Val104Asp
NM_001042704.2:c.311T>A	NP_001036169.1:p.Val104Asp
NM_001257139.2:c.229+916T>A	NP_001244068.1:n.229+916T>A