Canonical Allele Identifier: CA2697408536
Gene: CTSS HGNC NCBI

Linked Data

dbSNP Id: rs2101907295

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150733149_150733150insTTTCACAAGCCAGTATTCTTTCCCATTAAGATCACCAT , CM000663.2:g.150733149_150733150insTTTCACAAGCCAGTATTCTTTCCCATTAAGATCACCAT GRCh38
NC_000001.10:g.150705625_150705626insTTTCACAAGCCAGTATTCTTTCCCATTAAGATCACCAT , CM000663.1:g.150705625_150705626insTTTCACAAGCCAGTATTCTTTCCCATTAAGATCACCAT GRCh37
NC_000001.9:g.148972249_148972250insTTTCACAAGCCAGTATTCTTTCCCATTAAGATCACCAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368985.8:c.897-4_897-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA MANE Select ENSP00000357981.3:n.897-4_897-3insTGGTGATCTTAATGGGAAAGAATACTG...
ENST00000448301.7:c.669-4_669-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA ENSP00000408414.2:n.669-4_669-3insTGGTGATCTTAATGGGAAAGAATACTG...
ENST00000472977.7:c.897-4_897-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA ENSP00000475176.2:n.897-4_897-3insTGGTGATCTTAATGGGAAAGAATACTG...
ENST00000483930.2:c.*91-4_*91-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA ENSP00000475812.2:n.*91-4_*91-3insTGGTGATCTTAATGGGAAAGAATACTG...
ENST00000607427.2:c.897-4_897-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA ENSP00000475557.2:n.897-4_897-3insTGGTGATCTTAATGGGAAAGAATACTG...
ENST00000679512.1:c.794-4_794-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA ENSP00000505113.1:n.794-4_794-3insTGGTGATCTTAATGGGAAAGAATACTG...
ENST00000679898.1:c.624-4_624-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA ENSP00000505326.1:n.624-4_624-3insTGGTGATCTTAATGGGAAAGAATACTG...
ENST00000680288.1:c.747-4_747-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA ENSP00000506001.1:n.747-4_747-3insTGGTGATCTTAATGGGAAAGAATACTG...
ENST00000680311.1:c.628-4_628-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA ENSP00000505020.1:n.628-4_628-3insTGGTGATCTTAATGGGAAAGAATACTG...
ENST00000680471.1:c.*68-4_*68-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA ENSP00000506603.1:n.*68-4_*68-3insTGGTGATCTTAATGGGAAAGAATACTG...
ENST00000680664.1:c.720-4_720-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA ENSP00000506248.1:n.720-4_720-3insTGGTGATCTTAATGGGAAAGAATACTG...
ENST00000680931.1:c.*247-4_*247-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA ENSP00000504934.1:n.*247-4_*247-3insTGGTGATCTTAATGGGAAAGAATAC...
ENST00000681357.1:n.287-4_287-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA
ENST00000681444.1:c.897-4_897-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA ENSP00000505359.1:n.897-4_897-3insTGGTGATCTTAATGGGAAAGAATACTG...
ENST00000368985.7:c.897-4_897-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA ENSP00000357981.3:n.897-4_897-3insTGGTGATCTTAATGGGAAAGAATACTG...
ENST00000448301.6:c.747-4_747-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA ENSP00000408414.1:n.747-4_747-3insTGGTGATCTTAATGGGAAAGAATACTG...
ENST00000472977.6:c.190-4_190-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA
ENST00000483930.1:c.445-4_445-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA ENSP00000475812.1:n.445-4_445-3insTGGTGATCTTAATGGGAAAGAATACTG...
NM_001199739.1:c.747-4_747-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA NP_001186668.1:n.747-4_747-3insTGGTGATCTTAATGGGAAAGAATACTGGCT...
NM_004079.4:c.897-4_897-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA NP_004070.3:n.897-4_897-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGT...
NM_004079.5:c.897-4_897-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA MANE Select NP_004070.3:n.897-4_897-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGT...
NM_001199739.2:c.747-4_747-3insTGGTGATCTTAATGGGAAAGAATACTGGCTTGTGAAAA NP_001186668.1:n.747-4_747-3insTGGTGATCTTAATGGGAAAGAATACTGGCT...