Canonical Allele Identifier: CA342336690

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776663T>C (hg19) ; chr1:g.150804187T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804187T>C , CM000663.2:g.150804187T>C	GRCh38
NC_000001.10:g.150776663T>C , CM000663.1:g.150776663T>C	GRCh37
NC_000001.9:g.149043287T>C	NCBI36
NG_011848.1:g.9150A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.452A>G MANE Select	ENSP00000271651.3:p.Gln151Arg
ENST00000443913.2:c.629A>G	ENSP00000405083.2:p.Gln210Arg
ENST00000480670.2:n.3521A>G
ENST00000676680.1:c.452A>G	ENSP00000503270.1:p.Gln151Arg
ENST00000676716.1:c.329A>G	ENSP00000504737.1:p.Gln110Arg
ENST00000676751.1:c.452A>G	ENSP00000502964.1:p.Gln151Arg
ENST00000676824.1:c.452A>G	ENSP00000504176.1:p.Gln151Arg
ENST00000676966.1:c.452A>G	ENSP00000503723.1:p.Gln151Arg
ENST00000676970.1:c.452A>G	ENSP00000503832.1:p.Gln151Arg
ENST00000677330.1:n.2278A>G
ENST00000677611.1:n.304A>G
ENST00000677887.1:c.494A>G	ENSP00000503876.1:p.Gln165Arg
ENST00000678275.1:c.*344A>G	ENSP00000504796.1:n.*344A>G
ENST00000678337.1:c.488A>G	ENSP00000504759.1:p.Gln163Arg
ENST00000678725.1:n.1429A>G
ENST00000679090.1:n.1037A>G
ENST00000679148.1:n.3414A>G
ENST00000679171.1:n.2813A>G
ENST00000679260.1:c.399+1674A>G	ENSP00000504534.1:n.399+1674A>G
ENST00000271651.7:c.452A>G	ENSP00000271651.3:p.Gln151Arg
ENST00000443913.1:c.629A>G	ENSP00000405083.1:p.Gln210Arg
ENST00000480670.1:n.292A>G
NM_000396.3:c.452A>G	NP_000387.1:p.Gln151Arg
NM_000396.4:c.452A>G MANE Select	NP_000387.1:p.Gln151Arg