Canonical Allele Identifier: CA2479286203

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733117A= , CM000663.2:g.150733117A=	GRCh38
NC_000001.10:g.150705593A= , CM000663.1:g.150705593A=	GRCh37
NC_000001.9:g.148972217A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.925T= MANE Select	ENSP00000357981.3:p.Tyr309=
ENST00000448301.7:c.697T=	ENSP00000408414.2:p.Tyr233=
ENST00000472977.7:c.925T=	ENSP00000475176.2:p.Tyr309=
ENST00000483930.2:c.*119T=	ENSP00000475812.2:n.*119T=
ENST00000607427.2:c.925T=	ENSP00000475557.2:p.Tyr309=
ENST00000679512.1:c.822T=	ENSP00000505113.1:p.Asp274=
ENST00000679898.1:c.652T=	ENSP00000505326.1:p.Tyr218=
ENST00000680288.1:c.775T=	ENSP00000506001.1:p.Tyr259=
ENST00000680311.1:c.*8T=	ENSP00000505020.1:n.*8T=
ENST00000680471.1:c.*96T=	ENSP00000506603.1:n.*96T=
ENST00000680664.1:c.748T=	ENSP00000506248.1:p.Tyr250=
ENST00000680931.1:c.*275T=	ENSP00000504934.1:n.*275T=
ENST00000681357.1:n.315T=
ENST00000681444.1:c.925T=	ENSP00000505359.1:p.Tyr309=
ENST00000368985.7:c.925T=	ENSP00000357981.3:p.Tyr309=
ENST00000448301.6:c.775T=	ENSP00000408414.1:p.Tyr259=
ENST00000472977.6:c.218T=
ENST00000483930.1:c.473T=	ENSP00000475812.1:n.473T=
NM_001199739.1:c.775T=	NP_001186668.1:p.Tyr259=
NM_004079.4:c.925T=	NP_004070.3:p.Tyr309=
NM_004079.5:c.925T= MANE Select	NP_004070.3:p.Tyr309=
NM_001199739.2:c.775T=	NP_001186668.1:p.Tyr259=