Canonical Allele Identifier: CA2479286227

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150733214C= , CM000663.2:g.150733214C=	GRCh38
NC_000001.10:g.150705690C= , CM000663.1:g.150705690C=	GRCh37
NC_000001.9:g.148972314C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.897-69G= MANE Select	ENSP00000357981.3:n.897-69G=
ENST00000448301.7:c.669-69G=	ENSP00000408414.2:n.669-69G=
ENST00000472977.7:c.897-69G=	ENSP00000475176.2:n.897-69G=
ENST00000483930.2:c.*91-69G=	ENSP00000475812.2:n.*91-69G=
ENST00000607427.2:c.897-69G=	ENSP00000475557.2:n.897-69G=
ENST00000679512.1:c.794-69G=	ENSP00000505113.1:n.794-69G=
ENST00000679898.1:c.624-69G=	ENSP00000505326.1:n.624-69G=
ENST00000680288.1:c.747-69G=	ENSP00000506001.1:n.747-69G=
ENST00000680311.1:c.628-69G=	ENSP00000505020.1:n.628-69G=
ENST00000680471.1:c.*68-69G=	ENSP00000506603.1:n.*68-69G=
ENST00000680664.1:c.720-69G=	ENSP00000506248.1:n.720-69G=
ENST00000680931.1:c.*247-69G=	ENSP00000504934.1:n.*247-69G=
ENST00000681357.1:n.287-69G=
ENST00000681444.1:c.897-69G=	ENSP00000505359.1:n.897-69G=
ENST00000368985.7:c.897-69G=	ENSP00000357981.3:n.897-69G=
ENST00000448301.6:c.747-69G=	ENSP00000408414.1:n.747-69G=
ENST00000472977.6:c.190-69G=
ENST00000483930.1:c.445-69G=	ENSP00000475812.1:n.445-69G=
NM_001199739.1:c.747-69G=	NP_001186668.1:n.747-69G=
NM_004079.4:c.897-69G=	NP_004070.3:n.897-69G=
NM_004079.5:c.897-69G= MANE Select	NP_004070.3:n.897-69G=
NM_001199739.2:c.747-69G=	NP_001186668.1:n.747-69G=