Canonical Allele Identifier: CA2479286197

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733084A= , CM000663.2:g.150733084A=	GRCh38
NC_000001.10:g.150705560A= , CM000663.1:g.150705560A=	GRCh37
NC_000001.9:g.148972184A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.958T= MANE Select	ENSP00000357981.3:p.Cys320=
ENST00000448301.7:c.730T=	ENSP00000408414.2:p.Cys244=
ENST00000472977.7:c.958T=	ENSP00000475176.2:p.Cys320=
ENST00000483930.2:c.*152T=	ENSP00000475812.2:n.*152T=
ENST00000607427.2:c.958T=	ENSP00000475557.2:p.Cys320=
ENST00000679512.1:c.855T=	ENSP00000505113.1:p.Ile285=
ENST00000679898.1:c.685T=	ENSP00000505326.1:p.Cys229=
ENST00000680288.1:c.808T=	ENSP00000506001.1:p.Cys270=
ENST00000680311.1:c.*41T=	ENSP00000505020.1:n.*41T=
ENST00000680471.1:c.*129T=	ENSP00000506603.1:n.*129T=
ENST00000680664.1:c.781T=	ENSP00000506248.1:p.Cys261=
ENST00000680931.1:c.*308T=	ENSP00000504934.1:n.*308T=
ENST00000681357.1:n.348T=
ENST00000681444.1:c.958T=	ENSP00000505359.1:p.Cys320=
ENST00000368985.7:c.958T=	ENSP00000357981.3:p.Cys320=
ENST00000448301.6:c.808T=	ENSP00000408414.1:p.Cys270=
ENST00000472977.6:c.251T=
ENST00000483930.1:c.506T=	ENSP00000475812.1:n.506T=
NM_001199739.1:c.808T=	NP_001186668.1:p.Cys270=
NM_004079.4:c.958T=	NP_004070.3:p.Cys320=
NM_004079.5:c.958T= MANE Select	NP_004070.3:p.Cys320=
NM_001199739.2:c.808T=	NP_001186668.1:p.Cys270=