Canonical Allele Identifier: CA1142117075

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733109C= , CM000663.2:g.150733109C=	GRCh38
NC_000001.10:g.150705585C= , CM000663.1:g.150705585C=	GRCh37
NC_000001.9:g.148972209C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.933G= MANE Select	ENSP00000357981.3:p.Arg311=
ENST00000448301.7:c.705G=	ENSP00000408414.2:p.Arg235=
ENST00000472977.7:c.933G=	ENSP00000475176.2:p.Arg311=
ENST00000483930.2:c.*127G=	ENSP00000475812.2:n.*127G=
ENST00000607427.2:c.933G=	ENSP00000475557.2:p.Arg311=
ENST00000679512.1:c.830G=	ENSP00000505113.1:p.Gly277=
ENST00000679898.1:c.660G=	ENSP00000505326.1:p.Arg220=
ENST00000680288.1:c.783G=	ENSP00000506001.1:p.Arg261=
ENST00000680311.1:c.*16G=	ENSP00000505020.1:n.*16G=
ENST00000680471.1:c.*104G=	ENSP00000506603.1:n.*104G=
ENST00000680664.1:c.756G=	ENSP00000506248.1:p.Arg252=
ENST00000680931.1:c.*283G=	ENSP00000504934.1:n.*283G=
ENST00000681357.1:n.323G=
ENST00000681444.1:c.933G=	ENSP00000505359.1:p.Arg311=
ENST00000368985.7:c.933G=	ENSP00000357981.3:p.Arg311=
ENST00000448301.6:c.783G=	ENSP00000408414.1:p.Arg261=
ENST00000472977.6:c.226G=
ENST00000483930.1:c.481G=	ENSP00000475812.1:n.481G=
NM_001199739.1:c.783G=	NP_001186668.1:p.Arg261=
NM_004079.4:c.933G=	NP_004070.3:p.Arg311=
NM_004079.5:c.933G= MANE Select	NP_004070.3:p.Arg311=
NM_001199739.2:c.783G=	NP_001186668.1:p.Arg261=