Canonical Allele Identifier: CA342336376

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776522T>A (hg19) ; chr1:g.150804046T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804046T>A , CM000663.2:g.150804046T>A	GRCh38
NC_000001.10:g.150776522T>A , CM000663.1:g.150776522T>A	GRCh37
NC_000001.9:g.149043146T>A	NCBI36
NG_011848.1:g.9291A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.593A>T MANE Select	ENSP00000271651.3:p.Glu198Val
ENST00000443913.2:c.770A>T	ENSP00000405083.2:p.Glu257Val
ENST00000480670.2:n.3662A>T
ENST00000676680.1:c.593A>T	ENSP00000503270.1:p.Glu198Val
ENST00000676716.1:c.470A>T	ENSP00000504737.1:p.Glu157Val
ENST00000676751.1:c.593A>T	ENSP00000502964.1:p.Glu198Val
ENST00000676824.1:c.593A>T	ENSP00000504176.1:p.Glu198Val
ENST00000676966.1:c.593A>T	ENSP00000503723.1:p.Glu198Val
ENST00000676970.1:c.593A>T	ENSP00000503832.1:p.Glu198Val
ENST00000677330.1:n.2419A>T
ENST00000677611.1:n.445A>T
ENST00000677887.1:c.635A>T	ENSP00000503876.1:p.Glu212Val
ENST00000678275.1:c.*485A>T	ENSP00000504796.1:n.*485A>T
ENST00000678337.1:c.629A>T	ENSP00000504759.1:p.Glu210Val
ENST00000678725.1:n.1570A>T
ENST00000679090.1:n.1178A>T
ENST00000679148.1:n.3555A>T
ENST00000679171.1:n.2954A>T
ENST00000679260.1:c.399+1815A>T	ENSP00000504534.1:n.399+1815A>T
ENST00000271651.7:c.593A>T	ENSP00000271651.3:p.Glu198Val
ENST00000443913.1:c.770A>T	ENSP00000405083.1:p.Glu257Val
ENST00000480670.1:n.433A>T
NM_000396.3:c.593A>T	NP_000387.1:p.Glu198Val
NM_000396.4:c.593A>T MANE Select	NP_000387.1:p.Glu198Val