Canonical Allele Identifier: CA420699454

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776638G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804162G>A , CM000663.2:g.150804162G>A	GRCh38
NC_000001.10:g.150776638G>A , CM000663.1:g.150776638G>A	GRCh37
NC_000001.9:g.149043262G>A	NCBI36
NG_011848.1:g.9175C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.477C>T MANE Select	ENSP00000271651.3:p.Leu159=
ENST00000443913.2:c.654C>T	ENSP00000405083.2:p.Leu218=
ENST00000480670.2:n.3546C>T
ENST00000676680.1:c.477C>T	ENSP00000503270.1:p.Leu159=
ENST00000676716.1:c.354C>T	ENSP00000504737.1:p.Leu118=
ENST00000676751.1:c.477C>T	ENSP00000502964.1:p.Leu159=
ENST00000676824.1:c.477C>T	ENSP00000504176.1:p.Leu159=
ENST00000676966.1:c.477C>T	ENSP00000503723.1:p.Leu159=
ENST00000676970.1:c.477C>T	ENSP00000503832.1:p.Leu159=
ENST00000677330.1:n.2303C>T
ENST00000677611.1:n.329C>T
ENST00000677887.1:c.519C>T	ENSP00000503876.1:p.Leu173=
ENST00000678275.1:c.*369C>T	ENSP00000504796.1:n.*369C>T
ENST00000678337.1:c.513C>T	ENSP00000504759.1:p.Leu171=
ENST00000678725.1:n.1454C>T
ENST00000679090.1:n.1062C>T
ENST00000679148.1:n.3439C>T
ENST00000679171.1:n.2838C>T
ENST00000679260.1:c.399+1699C>T	ENSP00000504534.1:n.399+1699C>T
ENST00000271651.7:c.477C>T	ENSP00000271651.3:p.Leu159=
ENST00000443913.1:c.654C>T	ENSP00000405083.1:p.Leu218=
ENST00000480670.1:n.317C>T
NM_000396.3:c.477C>T	NP_000387.1:p.Leu159=
NM_000396.4:c.477C>T MANE Select	NP_000387.1:p.Leu159=