Canonical Allele Identifier: CA2479314245

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804239C= , CM000663.2:g.150804239C=	GRCh38
NC_000001.10:g.150776715C= , CM000663.1:g.150776715C=	GRCh37
NC_000001.9:g.149043339C=	NCBI36
NG_011848.1:g.9098G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.400G= MANE Select	ENSP00000271651.3:p.Gly134=
ENST00000443913.2:c.577G=	ENSP00000405083.2:p.Gly193=
ENST00000480670.2:n.3469G=
ENST00000676680.1:c.400G=	ENSP00000503270.1:p.Gly134=
ENST00000676716.1:c.277G=	ENSP00000504737.1:p.Gly93=
ENST00000676751.1:c.400G=	ENSP00000502964.1:p.Gly134=
ENST00000676824.1:c.400G=	ENSP00000504176.1:p.Gly134=
ENST00000676966.1:c.400G=	ENSP00000503723.1:p.Gly134=
ENST00000676970.1:c.400G=	ENSP00000503832.1:p.Gly134=
ENST00000677330.1:n.2226G=
ENST00000677611.1:n.252G=
ENST00000677887.1:c.442G=	ENSP00000503876.1:p.Gly148=
ENST00000678275.1:c.*292G=	ENSP00000504796.1:n.*292G=
ENST00000678337.1:c.436G=	ENSP00000504759.1:p.Gly146=
ENST00000678725.1:n.1377G=
ENST00000679090.1:n.985G=
ENST00000679148.1:n.3362G=
ENST00000679171.1:n.2761G=
ENST00000679260.1:c.399+1622G=	ENSP00000504534.1:n.399+1622G=
ENST00000271651.7:c.400G=	ENSP00000271651.3:p.Gly134=
ENST00000443913.1:c.577G=	ENSP00000405083.1:p.Gly193=
ENST00000480670.1:n.240G=
NM_000396.3:c.400G=	NP_000387.1:p.Gly134=
NM_000396.4:c.400G= MANE Select	NP_000387.1:p.Gly134=