Canonical Allele Identifier: CA2479286187
Gene: CTSS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150733023T= , CM000663.2:g.150733023T= GRCh38
NC_000001.10:g.150705499T= , CM000663.1:g.150705499T= GRCh37
NC_000001.9:g.148972123T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368985.8:c.*23A= MANE Select ENSP00000357981.3:n.*23A=
ENST00000448301.7:c.*23A= ENSP00000408414.2:n.*23A=
ENST00000472977.7:c.*23A= ENSP00000475176.2:n.*23A=
ENST00000483930.2:c.*213A= ENSP00000475812.2:n.*213A=
ENST00000607427.2:c.*23A= ENSP00000475557.2:n.*23A=
ENST00000679512.1:c.916A= ENSP00000505113.1:p.Asn306=
ENST00000679898.1:c.*23A= ENSP00000505326.1:n.*23A=
ENST00000680288.1:c.*23A= ENSP00000506001.1:n.*23A=
ENST00000680311.1:c.*102A= ENSP00000505020.1:n.*102A=
ENST00000680471.1:c.*190A= ENSP00000506603.1:n.*190A=
ENST00000680664.1:c.*23A= ENSP00000506248.1:n.*23A=
ENST00000680931.1:c.*369A= ENSP00000504934.1:n.*369A=
ENST00000681357.1:n.409A=
ENST00000681444.1:c.*23A= ENSP00000505359.1:n.*23A=
ENST00000368985.7:c.*23A= ENSP00000357981.3:n.*23A=
ENST00000448301.6:c.*23A= ENSP00000408414.1:n.*23A=
ENST00000472977.6:c.312A=
ENST00000483930.1:c.567A= ENSP00000475812.1:n.567A=
ENST00000607427.1:c.40A=
NM_001199739.1:c.*23A= NP_001186668.1:n.*23A=
NM_004079.4:c.*23A= NP_004070.3:n.*23A=
NM_004079.5:c.*23A= MANE Select NP_004070.3:n.*23A=
NM_001199739.2:c.*23A= NP_001186668.1:n.*23A=