Canonical Allele Identifier: CA2479286198

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733085A= , CM000663.2:g.150733085A=	GRCh38
NC_000001.10:g.150705561A= , CM000663.1:g.150705561A=	GRCh37
NC_000001.9:g.148972185A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.957T= MANE Select	ENSP00000357981.3:p.His319=
ENST00000448301.7:c.729T=	ENSP00000408414.2:p.His243=
ENST00000472977.7:c.957T=	ENSP00000475176.2:p.His319=
ENST00000483930.2:c.*151T=	ENSP00000475812.2:n.*151T=
ENST00000607427.2:c.957T=	ENSP00000475557.2:p.His319=
ENST00000679512.1:c.854T=	ENSP00000505113.1:p.Ile285=
ENST00000679898.1:c.684T=	ENSP00000505326.1:p.His228=
ENST00000680288.1:c.807T=	ENSP00000506001.1:p.His269=
ENST00000680311.1:c.*40T=	ENSP00000505020.1:n.*40T=
ENST00000680471.1:c.*128T=	ENSP00000506603.1:n.*128T=
ENST00000680664.1:c.780T=	ENSP00000506248.1:p.His260=
ENST00000680931.1:c.*307T=	ENSP00000504934.1:n.*307T=
ENST00000681357.1:n.347T=
ENST00000681444.1:c.957T=	ENSP00000505359.1:p.His319=
ENST00000368985.7:c.957T=	ENSP00000357981.3:p.His319=
ENST00000448301.6:c.807T=	ENSP00000408414.1:p.His269=
ENST00000472977.6:c.250T=
ENST00000483930.1:c.505T=	ENSP00000475812.1:n.505T=
NM_001199739.1:c.807T=	NP_001186668.1:p.His269=
NM_004079.4:c.957T=	NP_004070.3:p.His319=
NM_004079.5:c.957T= MANE Select	NP_004070.3:p.His319=
NM_001199739.2:c.807T=	NP_001186668.1:p.His269=