Canonical Allele Identifier: CA2479286201
Gene: CTSS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150733103T= , CM000663.2:g.150733103T= GRCh38
NC_000001.10:g.150705579T= , CM000663.1:g.150705579T= GRCh37
NC_000001.9:g.148972203T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368985.8:c.939A= MANE Select ENSP00000357981.3:p.Ala313=
ENST00000448301.7:c.711A= ENSP00000408414.2:p.Ala237=
ENST00000472977.7:c.939A= ENSP00000475176.2:p.Ala313=
ENST00000483930.2:c.*133A= ENSP00000475812.2:n.*133A=
ENST00000607427.2:c.939A= ENSP00000475557.2:p.Ala313=
ENST00000679512.1:c.836A= ENSP00000505113.1:p.Gln279=
ENST00000679898.1:c.666A= ENSP00000505326.1:p.Ala222=
ENST00000680288.1:c.789A= ENSP00000506001.1:p.Ala263=
ENST00000680311.1:c.*22A= ENSP00000505020.1:n.*22A=
ENST00000680471.1:c.*110A= ENSP00000506603.1:n.*110A=
ENST00000680664.1:c.762A= ENSP00000506248.1:p.Ala254=
ENST00000680931.1:c.*289A= ENSP00000504934.1:n.*289A=
ENST00000681357.1:n.329A=
ENST00000681444.1:c.939A= ENSP00000505359.1:p.Ala313=
ENST00000368985.7:c.939A= ENSP00000357981.3:p.Ala313=
ENST00000448301.6:c.789A= ENSP00000408414.1:p.Ala263=
ENST00000472977.6:c.232A=
ENST00000483930.1:c.487A= ENSP00000475812.1:n.487A=
NM_001199739.1:c.789A= NP_001186668.1:p.Ala263=
NM_004079.4:c.939A= NP_004070.3:p.Ala313=
NM_004079.5:c.939A= MANE Select NP_004070.3:p.Ala313=
NM_001199739.2:c.789A= NP_001186668.1:p.Ala263=