Canonical Allele Identifier: CA2479286177

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150732997A= , CM000663.2:g.150732997A=	GRCh38
NC_000001.10:g.150705473A= , CM000663.1:g.150705473A=	GRCh37
NC_000001.9:g.148972097A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*49T= MANE Select	ENSP00000357981.3:n.*49T=
ENST00000448301.7:c.*49T=	ENSP00000408414.2:n.*49T=
ENST00000472977.7:c.*49T=	ENSP00000475176.2:n.*49T=
ENST00000483930.2:c.*239T=	ENSP00000475812.2:n.*239T=
ENST00000607427.2:c.*49T=	ENSP00000475557.2:n.*49T=
ENST00000679512.1:c.*12T=	ENSP00000505113.1:n.*12T=
ENST00000679898.1:c.*49T=	ENSP00000505326.1:n.*49T=
ENST00000680288.1:c.*49T=	ENSP00000506001.1:n.*49T=
ENST00000680311.1:c.*128T=	ENSP00000505020.1:n.*128T=
ENST00000680471.1:c.*216T=	ENSP00000506603.1:n.*216T=
ENST00000680664.1:c.*49T=	ENSP00000506248.1:n.*49T=
ENST00000680931.1:c.*395T=	ENSP00000504934.1:n.*395T=
ENST00000681357.1:n.435T=
ENST00000681444.1:c.*49T=	ENSP00000505359.1:n.*49T=
ENST00000368985.7:c.*49T=	ENSP00000357981.3:n.*49T=
ENST00000448301.6:c.*49T=	ENSP00000408414.1:n.*49T=
ENST00000472977.6:c.338T=
ENST00000483930.1:c.593T=	ENSP00000475812.1:n.593T=
ENST00000607427.1:c.66T=
NM_001199739.1:c.*49T=	NP_001186668.1:n.*49T=
NM_004079.4:c.*49T=	NP_004070.3:n.*49T=
NM_004079.5:c.*49T= MANE Select	NP_004070.3:n.*49T=
NM_001199739.2:c.*49T=	NP_001186668.1:n.*49T=