Canonical Allele Identifier: CA2479314248

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804246G= , CM000663.2:g.150804246G=	GRCh38
NC_000001.10:g.150776722G= , CM000663.1:g.150776722G=	GRCh37
NC_000001.9:g.149043346G=	NCBI36
NG_011848.1:g.9091C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.400-7C= MANE Select	ENSP00000271651.3:n.400-7C=
ENST00000443913.2:c.577-7C=	ENSP00000405083.2:n.577-7C=
ENST00000480670.2:n.3469-7C=
ENST00000676680.1:c.400-7C=	ENSP00000503270.1:n.400-7C=
ENST00000676716.1:c.277-7C=	ENSP00000504737.1:n.277-7C=
ENST00000676751.1:c.400-7C=	ENSP00000502964.1:n.400-7C=
ENST00000676824.1:c.400-7C=	ENSP00000504176.1:n.400-7C=
ENST00000676966.1:c.400-7C=	ENSP00000503723.1:n.400-7C=
ENST00000676970.1:c.400-7C=	ENSP00000503832.1:n.400-7C=
ENST00000677330.1:n.2226-7C=
ENST00000677611.1:n.252-7C=
ENST00000677887.1:c.442-7C=	ENSP00000503876.1:n.442-7C=
ENST00000678275.1:c.*292-7C=	ENSP00000504796.1:n.*292-7C=
ENST00000678337.1:c.436-7C=	ENSP00000504759.1:n.436-7C=
ENST00000678725.1:n.1377-7C=
ENST00000679090.1:n.985-7C=
ENST00000679148.1:n.3355C=
ENST00000679171.1:n.2761-7C=
ENST00000679260.1:c.399+1615C=	ENSP00000504534.1:n.399+1615C=
ENST00000271651.7:c.400-7C=	ENSP00000271651.3:n.400-7C=
ENST00000443913.1:c.577-7C=	ENSP00000405083.1:n.577-7C=
ENST00000480670.1:n.240-7C=
NM_000396.3:c.400-7C=	NP_000387.1:n.400-7C=
NM_000396.4:c.400-7C= MANE Select	NP_000387.1:n.400-7C=