Canonical Allele Identifier: CA342335576

Gene: CTSK

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150796858C>G , CM000663.2:g.150796858C>G	GRCh38
NC_000001.10:g.150769334C>G , CM000663.1:g.150769334C>G	GRCh37
NC_000001.9:g.149035958C>G	NCBI36
NG_011848.1:g.16479G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.931G>C MANE Select	ENSP00000271651.3:p.Ala311Pro
ENST00000443913.2:c.1108G>C	ENSP00000405083.2:p.Ala370Pro
ENST00000480670.2:n.4000G>C
ENST00000676680.1:c.*225G>C	ENSP00000503270.1:n.*225G>C
ENST00000676716.1:c.808G>C	ENSP00000504737.1:p.Ala270Pro
ENST00000676751.1:c.825G>C	ENSP00000502964.1:p.Trp275Cys
ENST00000676824.1:c.931G>C	ENSP00000504176.1:p.Ala311Pro
ENST00000676966.1:c.931G>C	ENSP00000503723.1:p.Ala311Pro
ENST00000676970.1:c.943G>C	ENSP00000503832.1:p.Ala315Pro
ENST00000677330.1:n.2757G>C
ENST00000677611.1:n.783G>C
ENST00000677887.1:c.973G>C	ENSP00000503876.1:p.Ala325Pro
ENST00000678275.1:c.*823G>C	ENSP00000504796.1:n.*823G>C
ENST00000678337.1:c.967G>C	ENSP00000504759.1:p.Ala323Pro
ENST00000678725.1:n.2178G>C
ENST00000679090.1:n.1786G>C
ENST00000679148.1:n.3893G>C
ENST00000679171.1:n.3562G>C
ENST00000679178.1:n.642G>C
ENST00000679260.1:c.712G>C	ENSP00000504534.1:p.Ala238Pro
ENST00000271651.7:c.931G>C	ENSP00000271651.3:p.Ala311Pro
NM_000396.3:c.931G>C	NP_000387.1:p.Ala311Pro
NM_000396.4:c.931G>C MANE Select	NP_000387.1:p.Ala311Pro