Canonical Allele Identifier: CA2479286199

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733093C= , CM000663.2:g.150733093C=	GRCh38
NC_000001.10:g.150705569C= , CM000663.1:g.150705569C=	GRCh37
NC_000001.9:g.148972193C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.949G= MANE Select	ENSP00000357981.3:p.Gly317=
ENST00000448301.7:c.721G=	ENSP00000408414.2:p.Gly241=
ENST00000472977.7:c.949G=	ENSP00000475176.2:p.Gly317=
ENST00000483930.2:c.*143G=	ENSP00000475812.2:n.*143G=
ENST00000607427.2:c.949G=	ENSP00000475557.2:p.Gly317=
ENST00000679512.1:c.846G=	ENSP00000505113.1:p.Lys282=
ENST00000679898.1:c.676G=	ENSP00000505326.1:p.Gly226=
ENST00000680288.1:c.799G=	ENSP00000506001.1:p.Gly267=
ENST00000680311.1:c.*32G=	ENSP00000505020.1:n.*32G=
ENST00000680471.1:c.*120G=	ENSP00000506603.1:n.*120G=
ENST00000680664.1:c.772G=	ENSP00000506248.1:p.Gly258=
ENST00000680931.1:c.*299G=	ENSP00000504934.1:n.*299G=
ENST00000681357.1:n.339G=
ENST00000681444.1:c.949G=	ENSP00000505359.1:p.Gly317=
ENST00000368985.7:c.949G=	ENSP00000357981.3:p.Gly317=
ENST00000448301.6:c.799G=	ENSP00000408414.1:p.Gly267=
ENST00000472977.6:c.242G=
ENST00000483930.1:c.497G=	ENSP00000475812.1:n.497G=
NM_001199739.1:c.799G=	NP_001186668.1:p.Gly267=
NM_004079.4:c.949G=	NP_004070.3:p.Gly317=
NM_004079.5:c.949G= MANE Select	NP_004070.3:p.Gly317=
NM_001199739.2:c.799G=	NP_001186668.1:p.Gly267=