Canonical Allele Identifier: CA1143541530

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733006G= , CM000663.2:g.150733006G=	GRCh38
NC_000001.10:g.150705482G= , CM000663.1:g.150705482G=	GRCh37
NC_000001.9:g.148972106G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*40C= MANE Select	ENSP00000357981.3:n.*40C=
ENST00000448301.7:c.*40C=	ENSP00000408414.2:n.*40C=
ENST00000472977.7:c.*40C=	ENSP00000475176.2:n.*40C=
ENST00000483930.2:c.*230C=	ENSP00000475812.2:n.*230C=
ENST00000607427.2:c.*40C=	ENSP00000475557.2:n.*40C=
ENST00000679512.1:c.*3C=	ENSP00000505113.1:n.*3C=
ENST00000679898.1:c.*40C=	ENSP00000505326.1:n.*40C=
ENST00000680288.1:c.*40C=	ENSP00000506001.1:n.*40C=
ENST00000680311.1:c.*119C=	ENSP00000505020.1:n.*119C=
ENST00000680471.1:c.*207C=	ENSP00000506603.1:n.*207C=
ENST00000680664.1:c.*40C=	ENSP00000506248.1:n.*40C=
ENST00000680931.1:c.*386C=	ENSP00000504934.1:n.*386C=
ENST00000681357.1:n.426C=
ENST00000681444.1:c.*40C=	ENSP00000505359.1:n.*40C=
ENST00000368985.7:c.*40C=	ENSP00000357981.3:n.*40C=
ENST00000448301.6:c.*40C=	ENSP00000408414.1:n.*40C=
ENST00000472977.6:c.329C=
ENST00000483930.1:c.584C=	ENSP00000475812.1:n.584C=
ENST00000607427.1:c.57C=
NM_001199739.1:c.*40C=	NP_001186668.1:n.*40C=
NM_004079.4:c.*40C=	NP_004070.3:n.*40C=
NM_004079.5:c.*40C= MANE Select	NP_004070.3:n.*40C=
NM_001199739.2:c.*40C=	NP_001186668.1:n.*40C=