Canonical Allele Identifier: CA1140267368

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150754918G= , CM000663.2:g.150754918G=	GRCh38
NC_000001.10:g.150727394G= , CM000663.1:g.150727394G=	GRCh37
NC_000001.9:g.148994018G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.399+83C= MANE Select	ENSP00000357981.3:n.399+83C=
ENST00000448301.7:c.399+83C=	ENSP00000408414.2:n.399+83C=
ENST00000472977.7:c.399+83C=	ENSP00000475176.2:n.399+83C=
ENST00000480760.2:n.589C=
ENST00000483930.2:c.399+83C=	ENSP00000475812.2:n.399+83C=
ENST00000607427.2:c.399+83C=	ENSP00000475557.2:n.399+83C=
ENST00000679512.1:c.399+83C=	ENSP00000505113.1:n.399+83C=
ENST00000679582.1:c.399+83C=	ENSP00000504885.1:n.399+83C=
ENST00000679898.1:c.127-2910C=	ENSP00000505326.1:n.127-2910C=
ENST00000680288.1:c.250-2910C=	ENSP00000506001.1:n.250-2910C=
ENST00000680311.1:c.399+83C=	ENSP00000505020.1:n.399+83C=
ENST00000680471.1:c.399+83C=	ENSP00000506603.1:n.399+83C=
ENST00000680664.1:c.222+83C=	ENSP00000506248.1:n.222+83C=
ENST00000680931.1:c.399+83C=	ENSP00000504934.1:n.399+83C=
ENST00000681444.1:c.399+83C=	ENSP00000505359.1:n.399+83C=
ENST00000681728.1:c.399+83C=	ENSP00000505313.1:n.399+83C=
ENST00000368985.7:c.399+83C=	ENSP00000357981.3:n.399+83C=
ENST00000448301.6:c.250-2910C=	ENSP00000408414.1:n.250-2910C=
ENST00000480760.1:n.338+83C=
NM_001199739.1:c.250-2910C=	NP_001186668.1:n.250-2910C=
NM_004079.4:c.399+83C=	NP_004070.3:n.399+83C=
NM_004079.5:c.399+83C= MANE Select	NP_004070.3:n.399+83C=
NM_001199739.2:c.250-2910C=	NP_001186668.1:n.250-2910C=