Canonical Allele Identifier: CA2479286179

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733007C= , CM000663.2:g.150733007C=	GRCh38
NC_000001.10:g.150705483C= , CM000663.1:g.150705483C=	GRCh37
NC_000001.9:g.148972107C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*39G= MANE Select	ENSP00000357981.3:n.*39G=
ENST00000448301.7:c.*39G=	ENSP00000408414.2:n.*39G=
ENST00000472977.7:c.*39G=	ENSP00000475176.2:n.*39G=
ENST00000483930.2:c.*229G=	ENSP00000475812.2:n.*229G=
ENST00000607427.2:c.*39G=	ENSP00000475557.2:n.*39G=
ENST00000679512.1:c.*2G=	ENSP00000505113.1:n.*2G=
ENST00000679898.1:c.*39G=	ENSP00000505326.1:n.*39G=
ENST00000680288.1:c.*39G=	ENSP00000506001.1:n.*39G=
ENST00000680311.1:c.*118G=	ENSP00000505020.1:n.*118G=
ENST00000680471.1:c.*206G=	ENSP00000506603.1:n.*206G=
ENST00000680664.1:c.*39G=	ENSP00000506248.1:n.*39G=
ENST00000680931.1:c.*385G=	ENSP00000504934.1:n.*385G=
ENST00000681357.1:n.425G=
ENST00000681444.1:c.*39G=	ENSP00000505359.1:n.*39G=
ENST00000368985.7:c.*39G=	ENSP00000357981.3:n.*39G=
ENST00000448301.6:c.*39G=	ENSP00000408414.1:n.*39G=
ENST00000472977.6:c.328G=
ENST00000483930.1:c.583G=	ENSP00000475812.1:n.583G=
ENST00000607427.1:c.56G=
NM_001199739.1:c.*39G=	NP_001186668.1:n.*39G=
NM_004079.4:c.*39G=	NP_004070.3:n.*39G=
NM_004079.5:c.*39G= MANE Select	NP_004070.3:n.*39G=
NM_001199739.2:c.*39G=	NP_001186668.1:n.*39G=