Canonical Allele Identifier: CA338609682

Gene: CLCNKA

Linked Data

• gnomAD v4: 1-16024822-A-T
• MyVariant Identifiers: chr1:g.16351317A>T (hg19) ; chr1:g.16024822A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16024822A>T , CM000663.2:g.16024822A>T	GRCh38
NC_000001.10:g.16351317A>T , CM000663.1:g.16351317A>T	GRCh37
NC_000001.9:g.16223904A>T	NCBI36
NG_009359.1:g.7832A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331433.5:c.289A>T MANE Select	ENSP00000332771.4:p.Thr97Ser
ENST00000331433.4:c.289A>T	ENSP00000332771.4:p.Thr97Ser
ENST00000375692.5:c.289A>T	ENSP00000364844.1:p.Thr97Ser
ENST00000439316.6:c.229+894A>T	ENSP00000414445.2:n.229+894A>T
ENST00000464764.5:n.889-37A>T
ENST00000495784.1:n.447A>T
NM_001042704.1:c.289A>T	NP_001036169.1:p.Thr97Ser
NM_001257139.1:c.229+894A>T	NP_001244068.1:n.229+894A>T
NM_004070.3:c.289A>T	NP_004061.3:p.Thr97Ser
NM_004070.4:c.289A>T MANE Select	NP_004061.3:p.Thr97Ser
NM_001042704.2:c.289A>T	NP_001036169.1:p.Thr97Ser
NM_001257139.2:c.229+894A>T	NP_001244068.1:n.229+894A>T