Canonical Allele Identifier: CA420699497

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776698A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804222A>G , CM000663.2:g.150804222A>G	GRCh38
NC_000001.10:g.150776698A>G , CM000663.1:g.150776698A>G	GRCh37
NC_000001.9:g.149043322A>G	NCBI36
NG_011848.1:g.9115T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.417T>C MANE Select	ENSP00000271651.3:p.Cys139=
ENST00000443913.2:c.594T>C	ENSP00000405083.2:p.Cys198=
ENST00000480670.2:n.3486T>C
ENST00000676680.1:c.417T>C	ENSP00000503270.1:p.Cys139=
ENST00000676716.1:c.294T>C	ENSP00000504737.1:p.Cys98=
ENST00000676751.1:c.417T>C	ENSP00000502964.1:p.Cys139=
ENST00000676824.1:c.417T>C	ENSP00000504176.1:p.Cys139=
ENST00000676966.1:c.417T>C	ENSP00000503723.1:p.Cys139=
ENST00000676970.1:c.417T>C	ENSP00000503832.1:p.Cys139=
ENST00000677330.1:n.2243T>C
ENST00000677611.1:n.269T>C
ENST00000677887.1:c.459T>C	ENSP00000503876.1:p.Cys153=
ENST00000678275.1:c.*309T>C	ENSP00000504796.1:n.*309T>C
ENST00000678337.1:c.453T>C	ENSP00000504759.1:p.Cys151=
ENST00000678725.1:n.1394T>C
ENST00000679090.1:n.1002T>C
ENST00000679148.1:n.3379T>C
ENST00000679171.1:n.2778T>C
ENST00000679260.1:c.399+1639T>C	ENSP00000504534.1:n.399+1639T>C
ENST00000271651.7:c.417T>C	ENSP00000271651.3:p.Cys139=
ENST00000443913.1:c.594T>C	ENSP00000405083.1:p.Cys198=
ENST00000480670.1:n.257T>C
NM_000396.3:c.417T>C	NP_000387.1:p.Cys139=
NM_000396.4:c.417T>C MANE Select	NP_000387.1:p.Cys139=