Canonical Allele Identifier: CA2479314184

Gene: CTSK

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150804028A= , CM000663.2:g.150804028A=	GRCh38
NC_000001.10:g.150776504A= , CM000663.1:g.150776504A=	GRCh37
NC_000001.9:g.149043128A=	NCBI36
NG_011848.1:g.9309T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271651.8:c.611T= MANE Select	ENSP00000271651.3:p.Val204=
ENST00000443913.2:c.788T=	ENSP00000405083.2:p.Val263=
ENST00000480670.2:n.3680T=
ENST00000676680.1:c.611T=	ENSP00000503270.1:p.Val204=
ENST00000676716.1:c.488T=	ENSP00000504737.1:p.Val163=
ENST00000676751.1:c.611T=	ENSP00000502964.1:p.Val204=
ENST00000676824.1:c.611T=	ENSP00000504176.1:p.Val204=
ENST00000676966.1:c.611T=	ENSP00000503723.1:p.Val204=
ENST00000676970.1:c.611T=	ENSP00000503832.1:p.Val204=
ENST00000677330.1:n.2437T=
ENST00000677611.1:n.463T=
ENST00000677887.1:c.653T=	ENSP00000503876.1:p.Val218=
ENST00000678275.1:c.*503T=	ENSP00000504796.1:n.*503T=
ENST00000678337.1:c.647T=	ENSP00000504759.1:p.Val216=
ENST00000678725.1:n.1588T=
ENST00000679090.1:n.1196T=
ENST00000679148.1:n.3573T=
ENST00000679171.1:n.2972T=
ENST00000679260.1:c.399+1833T=	ENSP00000504534.1:n.399+1833T=
ENST00000271651.7:c.611T=	ENSP00000271651.3:p.Val204=
ENST00000480670.1:n.451T=
NM_000396.3:c.611T=	NP_000387.1:p.Val204=
NM_000396.4:c.611T= MANE Select	NP_000387.1:p.Val204=