Canonical Allele Identifier: CA342337707

Gene: CTSK

Linked Data

• dbSNP Id: rs2101954082
• MyVariant Identifiers: chr1:g.150779242A>C (hg19) ; chr1:g.150806766A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806766A>C , CM000663.2:g.150806766A>C	GRCh38
NC_000001.10:g.150779242A>C , CM000663.1:g.150779242A>C	GRCh37
NC_000001.9:g.149045866A>C	NCBI36
NG_011848.1:g.6571T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.40T>G MANE Select	ENSP00000271651.3:p.Phe14Val
ENST00000443913.2:c.217T>G	ENSP00000405083.2:p.Phe73Val
ENST00000480670.2:n.2648T>G
ENST00000676680.1:c.40T>G	ENSP00000503270.1:p.Phe14Val
ENST00000676716.1:c.40T>G	ENSP00000504737.1:p.Phe14Val
ENST00000676751.1:c.40T>G	ENSP00000502964.1:p.Phe14Val
ENST00000676824.1:c.40T>G	ENSP00000504176.1:p.Phe14Val
ENST00000676966.1:c.40T>G	ENSP00000503723.1:p.Phe14Val
ENST00000676970.1:c.40T>G	ENSP00000503832.1:p.Phe14Val
ENST00000677330.1:n.1405T>G
ENST00000677887.1:c.82T>G	ENSP00000503876.1:p.Phe28Val
ENST00000678275.1:c.40T>G	ENSP00000504796.1:p.Phe14Val
ENST00000678337.1:c.76T>G	ENSP00000504759.1:p.Phe26Val
ENST00000678725.1:n.1017T>G
ENST00000679090.1:n.164T>G
ENST00000679148.1:n.920T>G
ENST00000679171.1:n.1940T>G
ENST00000679260.1:c.40T>G	ENSP00000504534.1:p.Phe14Val
ENST00000271651.7:c.40T>G	ENSP00000271651.3:p.Phe14Val
ENST00000443913.1:c.217T>G	ENSP00000405083.1:p.Phe73Val
ENST00000480670.1:n.3T>G
NM_000396.3:c.40T>G	NP_000387.1:p.Phe14Val
NM_000396.4:c.40T>G MANE Select	NP_000387.1:p.Phe14Val