Canonical Allele Identifier: CA342336585

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776616G>C (hg19) ; chr1:g.150804140G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804140G>C , CM000663.2:g.150804140G>C	GRCh38
NC_000001.10:g.150776616G>C , CM000663.1:g.150776616G>C	GRCh37
NC_000001.9:g.149043240G>C	NCBI36
NG_011848.1:g.9197C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.499C>G MANE Select	ENSP00000271651.3:p.Leu167Val
ENST00000443913.2:c.676C>G	ENSP00000405083.2:p.Leu226Val
ENST00000480670.2:n.3568C>G
ENST00000676680.1:c.499C>G	ENSP00000503270.1:p.Leu167Val
ENST00000676716.1:c.376C>G	ENSP00000504737.1:p.Leu126Val
ENST00000676751.1:c.499C>G	ENSP00000502964.1:p.Leu167Val
ENST00000676824.1:c.499C>G	ENSP00000504176.1:p.Leu167Val
ENST00000676966.1:c.499C>G	ENSP00000503723.1:p.Leu167Val
ENST00000676970.1:c.499C>G	ENSP00000503832.1:p.Leu167Val
ENST00000677330.1:n.2325C>G
ENST00000677611.1:n.351C>G
ENST00000677887.1:c.541C>G	ENSP00000503876.1:p.Leu181Val
ENST00000678275.1:c.*391C>G	ENSP00000504796.1:n.*391C>G
ENST00000678337.1:c.535C>G	ENSP00000504759.1:p.Leu179Val
ENST00000678725.1:n.1476C>G
ENST00000679090.1:n.1084C>G
ENST00000679148.1:n.3461C>G
ENST00000679171.1:n.2860C>G
ENST00000679260.1:c.399+1721C>G	ENSP00000504534.1:n.399+1721C>G
ENST00000271651.7:c.499C>G	ENSP00000271651.3:p.Leu167Val
ENST00000443913.1:c.676C>G	ENSP00000405083.1:p.Leu226Val
ENST00000480670.1:n.339C>G
NM_000396.3:c.499C>G	NP_000387.1:p.Leu167Val
NM_000396.4:c.499C>G MANE Select	NP_000387.1:p.Leu167Val