Canonical Allele Identifier: CA1143464346

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733130A= , CM000663.2:g.150733130A=	GRCh38
NC_000001.10:g.150705606A= , CM000663.1:g.150705606A=	GRCh37
NC_000001.9:g.148972230A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.912T= MANE Select	ENSP00000357981.3:p.Phe304=
ENST00000448301.7:c.684T=	ENSP00000408414.2:p.Phe228=
ENST00000472977.7:c.912T=	ENSP00000475176.2:p.Phe304=
ENST00000483930.2:c.*106T=	ENSP00000475812.2:n.*106T=
ENST00000607427.2:c.912T=	ENSP00000475557.2:p.Phe304=
ENST00000679512.1:c.809T=	ENSP00000505113.1:p.Leu270=
ENST00000679898.1:c.639T=	ENSP00000505326.1:p.Phe213=
ENST00000680288.1:c.762T=	ENSP00000506001.1:p.Phe254=
ENST00000680311.1:c.643T=	ENSP00000505020.1:p.Trp215=
ENST00000680471.1:c.*83T=	ENSP00000506603.1:n.*83T=
ENST00000680664.1:c.735T=	ENSP00000506248.1:p.Phe245=
ENST00000680931.1:c.*262T=	ENSP00000504934.1:n.*262T=
ENST00000681357.1:n.302T=
ENST00000681444.1:c.912T=	ENSP00000505359.1:p.Phe304=
ENST00000368985.7:c.912T=	ENSP00000357981.3:p.Phe304=
ENST00000448301.6:c.762T=	ENSP00000408414.1:p.Phe254=
ENST00000472977.6:c.205T=
ENST00000483930.1:c.460T=	ENSP00000475812.1:n.460T=
NM_001199739.1:c.762T=	NP_001186668.1:p.Phe254=
NM_004079.4:c.912T=	NP_004070.3:p.Phe304=
NM_004079.5:c.912T= MANE Select	NP_004070.3:p.Phe304=
NM_001199739.2:c.762T=	NP_001186668.1:p.Phe254=