Canonical Allele Identifier: CA1141911572

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733111G= , CM000663.2:g.150733111G=	GRCh38
NC_000001.10:g.150705587G= , CM000663.1:g.150705587G=	GRCh37
NC_000001.9:g.148972211G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.931C= MANE Select	ENSP00000357981.3:p.Arg311=
ENST00000448301.7:c.703C=	ENSP00000408414.2:p.Arg235=
ENST00000472977.7:c.931C=	ENSP00000475176.2:p.Arg311=
ENST00000483930.2:c.*125C=	ENSP00000475812.2:n.*125C=
ENST00000607427.2:c.931C=	ENSP00000475557.2:p.Arg311=
ENST00000679512.1:c.828C=	ENSP00000505113.1:p.Phe276=
ENST00000679898.1:c.658C=	ENSP00000505326.1:p.Arg220=
ENST00000680288.1:c.781C=	ENSP00000506001.1:p.Arg261=
ENST00000680311.1:c.*14C=	ENSP00000505020.1:n.*14C=
ENST00000680471.1:c.*102C=	ENSP00000506603.1:n.*102C=
ENST00000680664.1:c.754C=	ENSP00000506248.1:p.Arg252=
ENST00000680931.1:c.*281C=	ENSP00000504934.1:n.*281C=
ENST00000681357.1:n.321C=
ENST00000681444.1:c.931C=	ENSP00000505359.1:p.Arg311=
ENST00000368985.7:c.931C=	ENSP00000357981.3:p.Arg311=
ENST00000448301.6:c.781C=	ENSP00000408414.1:p.Arg261=
ENST00000472977.6:c.224C=
ENST00000483930.1:c.479C=	ENSP00000475812.1:n.479C=
NM_001199739.1:c.781C=	NP_001186668.1:p.Arg261=
NM_004079.4:c.931C=	NP_004070.3:p.Arg311=
NM_004079.5:c.931C= MANE Select	NP_004070.3:p.Arg311=
NM_001199739.2:c.781C=	NP_001186668.1:p.Arg261=