Canonical Allele Identifier: CA2479286205

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733133G= , CM000663.2:g.150733133G=	GRCh38
NC_000001.10:g.150705609G= , CM000663.1:g.150705609G=	GRCh37
NC_000001.9:g.148972233G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.909C= MANE Select	ENSP00000357981.3:p.Asn303=
ENST00000448301.7:c.681C=	ENSP00000408414.2:p.Asn227=
ENST00000472977.7:c.909C=	ENSP00000475176.2:p.Asn303=
ENST00000483930.2:c.*103C=	ENSP00000475812.2:n.*103C=
ENST00000607427.2:c.909C=	ENSP00000475557.2:p.Asn303=
ENST00000679512.1:c.806C=	ENSP00000505113.1:p.Thr269=
ENST00000679898.1:c.636C=	ENSP00000505326.1:p.Asn212=
ENST00000680288.1:c.759C=	ENSP00000506001.1:p.Asn253=
ENST00000680311.1:c.640C=	ENSP00000505020.1:p.Leu214=
ENST00000680471.1:c.*80C=	ENSP00000506603.1:n.*80C=
ENST00000680664.1:c.732C=	ENSP00000506248.1:p.Asn244=
ENST00000680931.1:c.*259C=	ENSP00000504934.1:n.*259C=
ENST00000681357.1:n.299C=
ENST00000681444.1:c.909C=	ENSP00000505359.1:p.Asn303=
ENST00000368985.7:c.909C=	ENSP00000357981.3:p.Asn303=
ENST00000448301.6:c.759C=	ENSP00000408414.1:p.Asn253=
ENST00000472977.6:c.202C=
ENST00000483930.1:c.457C=	ENSP00000475812.1:n.457C=
NM_001199739.1:c.759C=	NP_001186668.1:p.Asn253=
NM_004079.4:c.909C=	NP_004070.3:p.Asn303=
NM_004079.5:c.909C= MANE Select	NP_004070.3:p.Asn303=
NM_001199739.2:c.759C=	NP_001186668.1:p.Asn253=