Canonical Allele Identifier: CA342337242

Gene: CTSK

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806132A>C , CM000663.2:g.150806132A>C	GRCh38
NC_000001.10:g.150778608A>C , CM000663.1:g.150778608A>C	GRCh37
NC_000001.9:g.149045232A>C	NCBI36
NG_011848.1:g.7205T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.213T>G MANE Select	ENSP00000271651.3:p.Tyr71Ter
ENST00000443913.2:c.390T>G	ENSP00000405083.2:p.Tyr130Ter
ENST00000480670.2:n.3282T>G
ENST00000676680.1:c.213T>G	ENSP00000503270.1:p.Tyr71Ter
ENST00000676716.1:c.121-116T>G	ENSP00000504737.1:n.121-116T>G
ENST00000676751.1:c.213T>G	ENSP00000502964.1:p.Tyr71Ter
ENST00000676824.1:c.213T>G	ENSP00000504176.1:p.Tyr71Ter
ENST00000676966.1:c.213T>G	ENSP00000503723.1:p.Tyr71Ter
ENST00000676970.1:c.213T>G	ENSP00000503832.1:p.Tyr71Ter
ENST00000677330.1:n.2039T>G
ENST00000677887.1:c.255T>G	ENSP00000503876.1:p.Tyr85Ter
ENST00000678275.1:c.*105T>G	ENSP00000504796.1:n.*105T>G
ENST00000678337.1:c.249T>G	ENSP00000504759.1:p.Tyr83Ter
ENST00000678725.1:n.1190T>G
ENST00000679090.1:n.798T>G
ENST00000679148.1:n.1554T>G
ENST00000679171.1:n.2574T>G
ENST00000679260.1:c.213T>G	ENSP00000504534.1:p.Tyr71Ter
ENST00000271651.7:c.213T>G	ENSP00000271651.3:p.Tyr71Ter
ENST00000443913.1:c.390T>G	ENSP00000405083.1:p.Tyr130Ter
ENST00000480670.1:n.84-116T>G
NM_000396.3:c.213T>G	NP_000387.1:p.Tyr71Ter
NM_000396.4:c.213T>G MANE Select	NP_000387.1:p.Tyr71Ter