Canonical Allele Identifier: CA420699465

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776656C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804180C>T , CM000663.2:g.150804180C>T	GRCh38
NC_000001.10:g.150776656C>T , CM000663.1:g.150776656C>T	GRCh37
NC_000001.9:g.149043280C>T	NCBI36
NG_011848.1:g.9157G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.459G>A MANE Select	ENSP00000271651.3:p.Lys153=
ENST00000443913.2:c.636G>A	ENSP00000405083.2:p.Lys212=
ENST00000480670.2:n.3528G>A
ENST00000676680.1:c.459G>A	ENSP00000503270.1:p.Lys153=
ENST00000676716.1:c.336G>A	ENSP00000504737.1:p.Lys112=
ENST00000676751.1:c.459G>A	ENSP00000502964.1:p.Lys153=
ENST00000676824.1:c.459G>A	ENSP00000504176.1:p.Lys153=
ENST00000676966.1:c.459G>A	ENSP00000503723.1:p.Lys153=
ENST00000676970.1:c.459G>A	ENSP00000503832.1:p.Lys153=
ENST00000677330.1:n.2285G>A
ENST00000677611.1:n.311G>A
ENST00000677887.1:c.501G>A	ENSP00000503876.1:p.Lys167=
ENST00000678275.1:c.*351G>A	ENSP00000504796.1:n.*351G>A
ENST00000678337.1:c.495G>A	ENSP00000504759.1:p.Lys165=
ENST00000678725.1:n.1436G>A
ENST00000679090.1:n.1044G>A
ENST00000679148.1:n.3421G>A
ENST00000679171.1:n.2820G>A
ENST00000679260.1:c.399+1681G>A	ENSP00000504534.1:n.399+1681G>A
ENST00000271651.7:c.459G>A	ENSP00000271651.3:p.Lys153=
ENST00000443913.1:c.636G>A	ENSP00000405083.1:p.Lys212=
ENST00000480670.1:n.299G>A
NM_000396.3:c.459G>A	NP_000387.1:p.Lys153=
NM_000396.4:c.459G>A MANE Select	NP_000387.1:p.Lys153=