Canonical Allele Identifier: CA2479314198

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804078T= , CM000663.2:g.150804078T=	GRCh38
NC_000001.10:g.150776554T= , CM000663.1:g.150776554T=	GRCh37
NC_000001.9:g.149043178T=	NCBI36
NG_011848.1:g.9259A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.561A= MANE Select	ENSP00000271651.3:p.Gln187=
ENST00000443913.2:c.738A=	ENSP00000405083.2:p.Gln246=
ENST00000480670.2:n.3630A=
ENST00000676680.1:c.561A=	ENSP00000503270.1:p.Gln187=
ENST00000676716.1:c.438A=	ENSP00000504737.1:p.Gln146=
ENST00000676751.1:c.561A=	ENSP00000502964.1:p.Gln187=
ENST00000676824.1:c.561A=	ENSP00000504176.1:p.Gln187=
ENST00000676966.1:c.561A=	ENSP00000503723.1:p.Gln187=
ENST00000676970.1:c.561A=	ENSP00000503832.1:p.Gln187=
ENST00000677330.1:n.2387A=
ENST00000677611.1:n.413A=
ENST00000677887.1:c.603A=	ENSP00000503876.1:p.Gln201=
ENST00000678275.1:c.*453A=	ENSP00000504796.1:n.*453A=
ENST00000678337.1:c.597A=	ENSP00000504759.1:p.Gln199=
ENST00000678725.1:n.1538A=
ENST00000679090.1:n.1146A=
ENST00000679148.1:n.3523A=
ENST00000679171.1:n.2922A=
ENST00000679260.1:c.399+1783A=	ENSP00000504534.1:n.399+1783A=
ENST00000271651.7:c.561A=	ENSP00000271651.3:p.Gln187=
ENST00000443913.1:c.738A=	ENSP00000405083.1:p.Gln246=
ENST00000480670.1:n.401A=
NM_000396.3:c.561A=	NP_000387.1:p.Gln187=
NM_000396.4:c.561A= MANE Select	NP_000387.1:p.Gln187=