Canonical Allele Identifier: CA420699508

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776701G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804225G>T , CM000663.2:g.150804225G>T	GRCh38
NC_000001.10:g.150776701G>T , CM000663.1:g.150776701G>T	GRCh37
NC_000001.9:g.149043325G>T	NCBI36
NG_011848.1:g.9112C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.414C>A MANE Select	ENSP00000271651.3:p.Ser138=
ENST00000443913.2:c.591C>A	ENSP00000405083.2:p.Ser197=
ENST00000480670.2:n.3483C>A
ENST00000676680.1:c.414C>A	ENSP00000503270.1:p.Ser138=
ENST00000676716.1:c.291C>A	ENSP00000504737.1:p.Ser97=
ENST00000676751.1:c.414C>A	ENSP00000502964.1:p.Ser138=
ENST00000676824.1:c.414C>A	ENSP00000504176.1:p.Ser138=
ENST00000676966.1:c.414C>A	ENSP00000503723.1:p.Ser138=
ENST00000676970.1:c.414C>A	ENSP00000503832.1:p.Ser138=
ENST00000677330.1:n.2240C>A
ENST00000677611.1:n.266C>A
ENST00000677887.1:c.456C>A	ENSP00000503876.1:p.Ser152=
ENST00000678275.1:c.*306C>A	ENSP00000504796.1:n.*306C>A
ENST00000678337.1:c.450C>A	ENSP00000504759.1:p.Ser150=
ENST00000678725.1:n.1391C>A
ENST00000679090.1:n.999C>A
ENST00000679148.1:n.3376C>A
ENST00000679171.1:n.2775C>A
ENST00000679260.1:c.399+1636C>A	ENSP00000504534.1:n.399+1636C>A
ENST00000271651.7:c.414C>A	ENSP00000271651.3:p.Ser138=
ENST00000443913.1:c.591C>A	ENSP00000405083.1:p.Ser197=
ENST00000480670.1:n.254C>A
NM_000396.3:c.414C>A	NP_000387.1:p.Ser138=
NM_000396.4:c.414C>A MANE Select	NP_000387.1:p.Ser138=