Canonical Allele Identifier: CA342336560

Gene: CTSK

Linked Data

• gnomAD v4: 1-150804129-A-C
• MyVariant Identifiers: chr1:g.150776605A>C (hg19) ; chr1:g.150804129A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804129A>C , CM000663.2:g.150804129A>C	GRCh38
NC_000001.10:g.150776605A>C , CM000663.1:g.150776605A>C	GRCh37
NC_000001.9:g.149043229A>C	NCBI36
NG_011848.1:g.9208T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.510T>G MANE Select	ENSP00000271651.3:p.Cys170Trp
ENST00000443913.2:c.687T>G	ENSP00000405083.2:p.Cys229Trp
ENST00000480670.2:n.3579T>G
ENST00000676680.1:c.510T>G	ENSP00000503270.1:p.Cys170Trp
ENST00000676716.1:c.387T>G	ENSP00000504737.1:p.Cys129Trp
ENST00000676751.1:c.510T>G	ENSP00000502964.1:p.Cys170Trp
ENST00000676824.1:c.510T>G	ENSP00000504176.1:p.Cys170Trp
ENST00000676966.1:c.510T>G	ENSP00000503723.1:p.Cys170Trp
ENST00000676970.1:c.510T>G	ENSP00000503832.1:p.Cys170Trp
ENST00000677330.1:n.2336T>G
ENST00000677611.1:n.362T>G
ENST00000677887.1:c.552T>G	ENSP00000503876.1:p.Cys184Trp
ENST00000678275.1:c.*402T>G	ENSP00000504796.1:n.*402T>G
ENST00000678337.1:c.546T>G	ENSP00000504759.1:p.Cys182Trp
ENST00000678725.1:n.1487T>G
ENST00000679090.1:n.1095T>G
ENST00000679148.1:n.3472T>G
ENST00000679171.1:n.2871T>G
ENST00000679260.1:c.399+1732T>G	ENSP00000504534.1:n.399+1732T>G
ENST00000271651.7:c.510T>G	ENSP00000271651.3:p.Cys170Trp
ENST00000443913.1:c.687T>G	ENSP00000405083.1:p.Cys229Trp
ENST00000480670.1:n.350T>G
NM_000396.3:c.510T>G	NP_000387.1:p.Cys170Trp
NM_000396.4:c.510T>G MANE Select	NP_000387.1:p.Cys170Trp