Canonical Allele Identifier: CA420699383

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776530A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804054A>T , CM000663.2:g.150804054A>T	GRCh38
NC_000001.10:g.150776530A>T , CM000663.1:g.150776530A>T	GRCh37
NC_000001.9:g.149043154A>T	NCBI36
NG_011848.1:g.9283T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.585T>A MANE Select	ENSP00000271651.3:p.Ile195=
ENST00000443913.2:c.762T>A	ENSP00000405083.2:p.Ile254=
ENST00000480670.2:n.3654T>A
ENST00000676680.1:c.585T>A	ENSP00000503270.1:p.Ile195=
ENST00000676716.1:c.462T>A	ENSP00000504737.1:p.Ile154=
ENST00000676751.1:c.585T>A	ENSP00000502964.1:p.Ile195=
ENST00000676824.1:c.585T>A	ENSP00000504176.1:p.Ile195=
ENST00000676966.1:c.585T>A	ENSP00000503723.1:p.Ile195=
ENST00000676970.1:c.585T>A	ENSP00000503832.1:p.Ile195=
ENST00000677330.1:n.2411T>A
ENST00000677611.1:n.437T>A
ENST00000677887.1:c.627T>A	ENSP00000503876.1:p.Ile209=
ENST00000678275.1:c.*477T>A	ENSP00000504796.1:n.*477T>A
ENST00000678337.1:c.621T>A	ENSP00000504759.1:p.Ile207=
ENST00000678725.1:n.1562T>A
ENST00000679090.1:n.1170T>A
ENST00000679148.1:n.3547T>A
ENST00000679171.1:n.2946T>A
ENST00000679260.1:c.399+1807T>A	ENSP00000504534.1:n.399+1807T>A
ENST00000271651.7:c.585T>A	ENSP00000271651.3:p.Ile195=
ENST00000443913.1:c.762T>A	ENSP00000405083.1:p.Ile254=
ENST00000480670.1:n.425T>A
NM_000396.3:c.585T>A	NP_000387.1:p.Ile195=
NM_000396.4:c.585T>A MANE Select	NP_000387.1:p.Ile195=