Canonical Allele Identifier: CA2647835183

Gene: CTSK

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150799159C>T , CM000663.2:g.150799159C>T	GRCh38
NC_000001.10:g.150771635C>T , CM000663.1:g.150771635C>T	GRCh37
NC_000001.9:g.149038259C>T	NCBI36
NG_011848.1:g.14178G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.890+9G>A MANE Select	ENSP00000271651.3:n.890+9G>A
ENST00000443913.2:c.1067+9G>A	ENSP00000405083.2:n.1067+9G>A
ENST00000480670.2:n.3959+9G>A
ENST00000676680.1:c.*184+9G>A	ENSP00000503270.1:n.*184+9G>A
ENST00000676716.1:c.767+9G>A	ENSP00000504737.1:n.767+9G>A
ENST00000676751.1:c.784+385G>A	ENSP00000502964.1:n.784+385G>A
ENST00000676824.1:c.890+9G>A	ENSP00000504176.1:n.890+9G>A
ENST00000676966.1:c.890+9G>A	ENSP00000503723.1:n.890+9G>A
ENST00000676970.1:c.902+9G>A	ENSP00000503832.1:n.902+9G>A
ENST00000677330.1:n.2716+9G>A
ENST00000677611.1:n.742+9G>A
ENST00000677887.1:c.932+9G>A	ENSP00000503876.1:n.932+9G>A
ENST00000678275.1:c.*782+9G>A	ENSP00000504796.1:n.*782+9G>A
ENST00000678337.1:c.926+9G>A	ENSP00000504759.1:n.926+9G>A
ENST00000678725.1:n.2137+9G>A
ENST00000679090.1:n.1745+9G>A
ENST00000679148.1:n.3852+9G>A
ENST00000679171.1:n.3521+9G>A
ENST00000679178.1:n.601+9G>A
ENST00000679260.1:c.671+9G>A	ENSP00000504534.1:n.671+9G>A
ENST00000271651.7:c.890+9G>A	ENSP00000271651.3:n.890+9G>A
NM_000396.3:c.890+9G>A	NP_000387.1:n.890+9G>A
NM_000396.4:c.890+9G>A MANE Select	NP_000387.1:n.890+9G>A