Canonical Allele Identifier: CA342336765

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776697A>G (hg19) ; chr1:g.150804221A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804221A>G , CM000663.2:g.150804221A>G	GRCh38
NC_000001.10:g.150776697A>G , CM000663.1:g.150776697A>G	GRCh37
NC_000001.9:g.149043321A>G	NCBI36
NG_011848.1:g.9116T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.418T>C MANE Select	ENSP00000271651.3:p.Trp140Arg
ENST00000443913.2:c.595T>C	ENSP00000405083.2:p.Trp199Arg
ENST00000480670.2:n.3487T>C
ENST00000676680.1:c.418T>C	ENSP00000503270.1:p.Trp140Arg
ENST00000676716.1:c.295T>C	ENSP00000504737.1:p.Trp99Arg
ENST00000676751.1:c.418T>C	ENSP00000502964.1:p.Trp140Arg
ENST00000676824.1:c.418T>C	ENSP00000504176.1:p.Trp140Arg
ENST00000676966.1:c.418T>C	ENSP00000503723.1:p.Trp140Arg
ENST00000676970.1:c.418T>C	ENSP00000503832.1:p.Trp140Arg
ENST00000677330.1:n.2244T>C
ENST00000677611.1:n.270T>C
ENST00000677887.1:c.460T>C	ENSP00000503876.1:p.Trp154Arg
ENST00000678275.1:c.*310T>C	ENSP00000504796.1:n.*310T>C
ENST00000678337.1:c.454T>C	ENSP00000504759.1:p.Trp152Arg
ENST00000678725.1:n.1395T>C
ENST00000679090.1:n.1003T>C
ENST00000679148.1:n.3380T>C
ENST00000679171.1:n.2779T>C
ENST00000679260.1:c.399+1640T>C	ENSP00000504534.1:n.399+1640T>C
ENST00000271651.7:c.418T>C	ENSP00000271651.3:p.Trp140Arg
ENST00000443913.1:c.595T>C	ENSP00000405083.1:p.Trp199Arg
ENST00000480670.1:n.258T>C
NM_000396.3:c.418T>C	NP_000387.1:p.Trp140Arg
NM_000396.4:c.418T>C MANE Select	NP_000387.1:p.Trp140Arg