Canonical Allele Identifier: CA342337692

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150779235A>C (hg19) ; chr1:g.150806759A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806759A>C , CM000663.2:g.150806759A>C	GRCh38
NC_000001.10:g.150779235A>C , CM000663.1:g.150779235A>C	GRCh37
NC_000001.9:g.149045859A>C	NCBI36
NG_011848.1:g.6578T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.47T>G MANE Select	ENSP00000271651.3:p.Leu16Arg
ENST00000443913.2:c.224T>G	ENSP00000405083.2:p.Leu75Arg
ENST00000480670.2:n.2655T>G
ENST00000676680.1:c.47T>G	ENSP00000503270.1:p.Leu16Arg
ENST00000676716.1:c.47T>G	ENSP00000504737.1:p.Leu16Arg
ENST00000676751.1:c.47T>G	ENSP00000502964.1:p.Leu16Arg
ENST00000676824.1:c.47T>G	ENSP00000504176.1:p.Leu16Arg
ENST00000676966.1:c.47T>G	ENSP00000503723.1:p.Leu16Arg
ENST00000676970.1:c.47T>G	ENSP00000503832.1:p.Leu16Arg
ENST00000677330.1:n.1412T>G
ENST00000677887.1:c.89T>G	ENSP00000503876.1:p.Leu30Arg
ENST00000678275.1:c.47T>G	ENSP00000504796.1:p.Leu16Arg
ENST00000678337.1:c.83T>G	ENSP00000504759.1:p.Leu28Arg
ENST00000678725.1:n.1024T>G
ENST00000679090.1:n.171T>G
ENST00000679148.1:n.927T>G
ENST00000679171.1:n.1947T>G
ENST00000679260.1:c.47T>G	ENSP00000504534.1:p.Leu16Arg
ENST00000271651.7:c.47T>G	ENSP00000271651.3:p.Leu16Arg
ENST00000443913.1:c.224T>G	ENSP00000405083.1:p.Leu75Arg
ENST00000480670.1:n.10T>G
NM_000396.3:c.47T>G	NP_000387.1:p.Leu16Arg
NM_000396.4:c.47T>G MANE Select	NP_000387.1:p.Leu16Arg