Canonical Allele Identifier: CA420706385

Gene: CTSK

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150796871T>G , CM000663.2:g.150796871T>G	GRCh38
NC_000001.10:g.150769347T>G , CM000663.1:g.150769347T>G	GRCh37
NC_000001.9:g.149035971T>G	NCBI36
NG_011848.1:g.16466A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.918A>C MANE Select	ENSP00000271651.3:p.Gly306=
ENST00000443913.2:c.1095A>C	ENSP00000405083.2:p.Gly365=
ENST00000480670.2:n.3987A>C
ENST00000676680.1:c.*212A>C	ENSP00000503270.1:n.*212A>C
ENST00000676716.1:c.795A>C	ENSP00000504737.1:p.Gly265=
ENST00000676751.1:c.812A>C	ENSP00000502964.1:p.Asp271Ala
ENST00000676824.1:c.918A>C	ENSP00000504176.1:p.Gly306=
ENST00000676966.1:c.918A>C	ENSP00000503723.1:p.Gly306=
ENST00000676970.1:c.930A>C	ENSP00000503832.1:p.Gly310=
ENST00000677330.1:n.2744A>C
ENST00000677611.1:n.770A>C
ENST00000677887.1:c.960A>C	ENSP00000503876.1:p.Gly320=
ENST00000678275.1:c.*810A>C	ENSP00000504796.1:n.*810A>C
ENST00000678337.1:c.954A>C	ENSP00000504759.1:p.Gly318=
ENST00000678725.1:n.2165A>C
ENST00000679090.1:n.1773A>C
ENST00000679148.1:n.3880A>C
ENST00000679171.1:n.3549A>C
ENST00000679178.1:n.629A>C
ENST00000679260.1:c.699A>C	ENSP00000504534.1:p.Gly233=
ENST00000271651.7:c.918A>C	ENSP00000271651.3:p.Gly306=
NM_000396.3:c.918A>C	NP_000387.1:p.Gly306=
NM_000396.4:c.918A>C MANE Select	NP_000387.1:p.Gly306=