Canonical Allele Identifier: CA342336759

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776695C>G (hg19) ; chr1:g.150804219C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804219C>G , CM000663.2:g.150804219C>G	GRCh38
NC_000001.10:g.150776695C>G , CM000663.1:g.150776695C>G	GRCh37
NC_000001.9:g.149043319C>G	NCBI36
NG_011848.1:g.9118G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.420G>C MANE Select	ENSP00000271651.3:p.Trp140Cys
ENST00000443913.2:c.597G>C	ENSP00000405083.2:p.Trp199Cys
ENST00000480670.2:n.3489G>C
ENST00000676680.1:c.420G>C	ENSP00000503270.1:p.Trp140Cys
ENST00000676716.1:c.297G>C	ENSP00000504737.1:p.Trp99Cys
ENST00000676751.1:c.420G>C	ENSP00000502964.1:p.Trp140Cys
ENST00000676824.1:c.420G>C	ENSP00000504176.1:p.Trp140Cys
ENST00000676966.1:c.420G>C	ENSP00000503723.1:p.Trp140Cys
ENST00000676970.1:c.420G>C	ENSP00000503832.1:p.Trp140Cys
ENST00000677330.1:n.2246G>C
ENST00000677611.1:n.272G>C
ENST00000677887.1:c.462G>C	ENSP00000503876.1:p.Trp154Cys
ENST00000678275.1:c.*312G>C	ENSP00000504796.1:n.*312G>C
ENST00000678337.1:c.456G>C	ENSP00000504759.1:p.Trp152Cys
ENST00000678725.1:n.1397G>C
ENST00000679090.1:n.1005G>C
ENST00000679148.1:n.3382G>C
ENST00000679171.1:n.2781G>C
ENST00000679260.1:c.399+1642G>C	ENSP00000504534.1:n.399+1642G>C
ENST00000271651.7:c.420G>C	ENSP00000271651.3:p.Trp140Cys
ENST00000443913.1:c.597G>C	ENSP00000405083.1:p.Trp199Cys
ENST00000480670.1:n.260G>C
NM_000396.3:c.420G>C	NP_000387.1:p.Trp140Cys
NM_000396.4:c.420G>C MANE Select	NP_000387.1:p.Trp140Cys