Canonical Allele Identifier: CA2573895578

Gene: CTSS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150732973del , CM000663.2:g.150732973del	GRCh38
NC_000001.10:g.150705449del , CM000663.1:g.150705449del	GRCh37
NC_000001.9:g.148972073del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368985.8:c.*74del MANE Select	ENSP00000357981.3:n.*74del
ENST00000448301.7:c.*74del	ENSP00000408414.2:n.*74del
ENST00000472977.7:c.*74del	ENSP00000475176.2:n.*74del
ENST00000483930.2:c.*264del	ENSP00000475812.2:n.*264del
ENST00000607427.2:c.*74del	ENSP00000475557.2:n.*74del
ENST00000679512.1:c.*37del	ENSP00000505113.1:n.*37del
ENST00000679898.1:c.*74del	ENSP00000505326.1:n.*74del
ENST00000680288.1:c.*74del	ENSP00000506001.1:n.*74del
ENST00000680311.1:c.*153del	ENSP00000505020.1:n.*153del
ENST00000680471.1:c.*241del	ENSP00000506603.1:n.*241del
ENST00000680664.1:c.*74del	ENSP00000506248.1:n.*74del
ENST00000680931.1:c.*420del	ENSP00000504934.1:n.*420del
ENST00000681357.1:n.460del
ENST00000681444.1:c.*74del	ENSP00000505359.1:n.*74del
ENST00000368985.7:c.*74del	ENSP00000357981.3:n.*74del
ENST00000448301.6:c.*74del	ENSP00000408414.1:n.*74del
ENST00000472977.6:c.363del
ENST00000483930.1:c.618del	ENSP00000475812.1:n.618del
ENST00000607427.1:c.91del
NM_001199739.1:c.*74del	NP_001186668.1:n.*74del
NM_004079.4:c.*74del	NP_004070.3:n.*74del
NM_004079.5:c.*74del MANE Select	NP_004070.3:n.*74del
NM_001199739.2:c.*74del	NP_001186668.1:n.*74del