Canonical Allele Identifier: CA420701499

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150779255T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150806779T>C , CM000663.2:g.150806779T>C	GRCh38
NC_000001.10:g.150779255T>C , CM000663.1:g.150779255T>C	GRCh37
NC_000001.9:g.149045879T>C	NCBI36
NG_011848.1:g.6558A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.27A>G MANE Select	ENSP00000271651.3:p.Leu9=
ENST00000443913.2:c.204A>G	ENSP00000405083.2:p.Leu68=
ENST00000480670.2:n.2635A>G
ENST00000676680.1:c.27A>G	ENSP00000503270.1:p.Leu9=
ENST00000676716.1:c.27A>G	ENSP00000504737.1:p.Leu9=
ENST00000676751.1:c.27A>G	ENSP00000502964.1:p.Leu9=
ENST00000676824.1:c.27A>G	ENSP00000504176.1:p.Leu9=
ENST00000676966.1:c.27A>G	ENSP00000503723.1:p.Leu9=
ENST00000676970.1:c.27A>G	ENSP00000503832.1:p.Leu9=
ENST00000677330.1:n.1392A>G
ENST00000677887.1:c.69A>G	ENSP00000503876.1:p.Leu23=
ENST00000678275.1:c.27A>G	ENSP00000504796.1:p.Leu9=
ENST00000678337.1:c.63A>G	ENSP00000504759.1:p.Leu21=
ENST00000678725.1:n.1004A>G
ENST00000679090.1:n.151A>G
ENST00000679148.1:n.907A>G
ENST00000679171.1:n.1927A>G
ENST00000679260.1:c.27A>G	ENSP00000504534.1:p.Leu9=
ENST00000271651.7:c.27A>G	ENSP00000271651.3:p.Leu9=
ENST00000443913.1:c.204A>G	ENSP00000405083.1:p.Leu68=
NM_000396.3:c.27A>G	NP_000387.1:p.Leu9=
NM_000396.4:c.27A>G MANE Select	NP_000387.1:p.Leu9=