Canonical Allele Identifier: CA342336543

Gene: CTSK

Linked Data

• MyVariant Identifiers: chr1:g.150776597T>A (hg19) ; chr1:g.150804121T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804121T>A , CM000663.2:g.150804121T>A	GRCh38
NC_000001.10:g.150776597T>A , CM000663.1:g.150776597T>A	GRCh37
NC_000001.9:g.149043221T>A	NCBI36
NG_011848.1:g.9216A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000271651.8:c.518A>T MANE Select	ENSP00000271651.3:p.Glu173Val
ENST00000443913.2:c.695A>T	ENSP00000405083.2:p.Glu232Val
ENST00000480670.2:n.3587A>T
ENST00000676680.1:c.518A>T	ENSP00000503270.1:p.Glu173Val
ENST00000676716.1:c.395A>T	ENSP00000504737.1:p.Glu132Val
ENST00000676751.1:c.518A>T	ENSP00000502964.1:p.Glu173Val
ENST00000676824.1:c.518A>T	ENSP00000504176.1:p.Glu173Val
ENST00000676966.1:c.518A>T	ENSP00000503723.1:p.Glu173Val
ENST00000676970.1:c.518A>T	ENSP00000503832.1:p.Glu173Val
ENST00000677330.1:n.2344A>T
ENST00000677611.1:n.370A>T
ENST00000677887.1:c.560A>T	ENSP00000503876.1:p.Glu187Val
ENST00000678275.1:c.*410A>T	ENSP00000504796.1:n.*410A>T
ENST00000678337.1:c.554A>T	ENSP00000504759.1:p.Glu185Val
ENST00000678725.1:n.1495A>T
ENST00000679090.1:n.1103A>T
ENST00000679148.1:n.3480A>T
ENST00000679171.1:n.2879A>T
ENST00000679260.1:c.399+1740A>T	ENSP00000504534.1:n.399+1740A>T
ENST00000271651.7:c.518A>T	ENSP00000271651.3:p.Glu173Val
ENST00000443913.1:c.695A>T	ENSP00000405083.1:p.Glu232Val
ENST00000480670.1:n.358A>T
NM_000396.3:c.518A>T	NP_000387.1:p.Glu173Val
NM_000396.4:c.518A>T MANE Select	NP_000387.1:p.Glu173Val