Canonical Allele Identifier: CA342335824

Gene: CTSK

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150799228G>T , CM000663.2:g.150799228G>T	GRCh38
NC_000001.10:g.150771704G>T , CM000663.1:g.150771704G>T	GRCh37
NC_000001.9:g.149038328G>T	NCBI36
NG_011848.1:g.14109C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.830C>A MANE Select	ENSP00000271651.3:p.Ala277Glu
ENST00000443913.2:c.1007C>A	ENSP00000405083.2:p.Ala336Glu
ENST00000480670.2:n.3899C>A
ENST00000676680.1:c.*124C>A	ENSP00000503270.1:n.*124C>A
ENST00000676716.1:c.707C>A	ENSP00000504737.1:p.Ala236Glu
ENST00000676751.1:c.784+316C>A	ENSP00000502964.1:n.784+316C>A
ENST00000676824.1:c.830C>A	ENSP00000504176.1:p.Ala277Glu
ENST00000676966.1:c.830C>A	ENSP00000503723.1:p.Ala277Glu
ENST00000676970.1:c.842C>A	ENSP00000503832.1:p.Ala281Glu
ENST00000677330.1:n.2656C>A
ENST00000677611.1:n.682C>A
ENST00000677887.1:c.872C>A	ENSP00000503876.1:p.Ala291Glu
ENST00000678275.1:c.*722C>A	ENSP00000504796.1:n.*722C>A
ENST00000678337.1:c.866C>A	ENSP00000504759.1:p.Ala289Glu
ENST00000678725.1:n.2077C>A
ENST00000679090.1:n.1685C>A
ENST00000679148.1:n.3792C>A
ENST00000679171.1:n.3461C>A
ENST00000679178.1:n.541C>A
ENST00000679260.1:c.611C>A	ENSP00000504534.1:p.Ala204Glu
ENST00000271651.7:c.830C>A	ENSP00000271651.3:p.Ala277Glu
NM_000396.3:c.830C>A	NP_000387.1:p.Ala277Glu
NM_000396.4:c.830C>A MANE Select	NP_000387.1:p.Ala277Glu