Canonical Allele Identifier: CA2737032460
Gene: CTSA HGNC NCBI

Linked Data

dbSNP Id: rs2145816074

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45892862dup , CM000682.2:g.45892862dup GRCh38
NC_000020.10:g.44521501dup , CM000682.1:g.44521501dup GRCh37
NC_000020.9:g.43954908dup NCBI36
NG_008291.1:g.6911dup
NG_033108.1:g.3426dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000480961.3:n.999dup
ENST00000484855.4:n.632dup
ENST00000493522.8:n.610dup
ENST00000606066.3:n.1073dup
ENST00000606782.3:n.703dup
ENST00000607187.3:n.999dup
ENST00000607212.3:n.793dup
ENST00000607814.7:n.1318dup
ENST00000677755.2:n.1002dup
ENST00000678622.2:n.999dup
ENST00000678691.2:n.999dup
ENST00000678988.2:n.1621dup
ENST00000679053.2:n.999dup
ENST00000679343.2:n.999dup
ENST00000684198.1:n.999dup
ENST00000372459.7:c.582dup ENSP00000361537.2:p.Pro195SerfsTer18
ENST00000372484.8:c.636dup ENSP00000361562.3:p.Pro213SerfsTer18
ENST00000419493.3:c.582dup ENSP00000408533.3:p.Pro195SerfsTer18
ENST00000480961.2:n.609dup
ENST00000484855.3:n.632dup
ENST00000493522.7:n.610dup
ENST00000606066.2:n.721dup
ENST00000606394.6:c.*224dup ENSP00000475827.1:n.*224dup
ENST00000606782.2:n.703dup
ENST00000607187.2:n.513dup
ENST00000607212.2:n.793dup
ENST00000607482.6:c.582dup ENSP00000475524.2:p.Pro195SerfsTer18
ENST00000607814.6:n.1318dup
ENST00000646241.3:c.582dup MANE Select ENSP00000493613.2:p.Pro195SerfsTer18
ENST00000676526.1:c.636dup ENSP00000504209.1:p.Pro213SerfsTer?
ENST00000676597.1:c.582dup ENSP00000503904.1:p.Pro195SerfsTer18
ENST00000676657.1:c.582dup ENSP00000504158.1:p.Pro195SerfsTer?
ENST00000676967.1:c.582dup ENSP00000502866.1:p.Pro195SerfsTer?
ENST00000677394.1:c.636dup ENSP00000504790.1:p.Pro213SerfsTer18
ENST00000677525.1:c.*405dup ENSP00000504197.1:n.*405dup
ENST00000677755.1:n.1002dup
ENST00000678025.1:c.582dup ENSP00000503463.1:p.Pro195SerfsTer?
ENST00000678078.1:c.636dup ENSP00000502993.1:p.Pro213SerfsTer?
ENST00000678217.1:c.582dup ENSP00000504109.1:p.Pro195SerfsTer18
ENST00000678331.1:c.582dup ENSP00000504524.1:p.Pro195SerfsTer18
ENST00000678443.1:c.582dup ENSP00000504006.1:p.Pro195SerfsTer18
ENST00000678512.1:n.846dup
ENST00000678622.1:n.627dup
ENST00000678691.1:n.460dup
ENST00000678939.1:c.582dup ENSP00000503404.1:p.Pro195SerfsTer18
ENST00000678988.1:n.1621dup
ENST00000679053.1:n.627dup
ENST00000679343.1:n.620dup
ENST00000191018.9:c.582dup ENSP00000191018.5:p.Pro195SerfsTer18
ENST00000354880.9:c.585dup ENSP00000346952.4:p.Pro196SerfsTer18
ENST00000372459.6:c.582dup ENSP00000361537.2:p.Pro195SerfsTer18
ENST00000372484.7:c.636dup ENSP00000361562.3:p.Pro213SerfsTer18
ENST00000419493.2:c.111dup ENSP00000408533.2:p.Pro38SerfsTer18
ENST00000485627.1:n.243dup
ENST00000606394.5:c.*224dup ENSP00000475827.1:n.*224dup
ENST00000606782.1:n.215dup
ENST00000606788.5:c.636dup ENSP00000476235.1:p.Pro213SerfsTer?
NM_000308.2:c.636dup NP_000299.2:p.Pro213SerfsTer18
NM_000308.3:c.636dup NP_000299.2:p.Pro213SerfsTer18
NM_001127695.1:c.582dup NP_001121167.1:p.Pro195SerfsTer18
NM_001127695.2:c.582dup NP_001121167.1:p.Pro195SerfsTer18
NM_001167594.1:c.585dup NP_001161066.1:p.Pro196SerfsTer18
NM_001167594.2:c.585dup NP_001161066.1:p.Pro196SerfsTer18
NR_133656.1:n.1818dup
NM_000308.4:c.582dup MANE Select NP_000299.3:p.Pro195SerfsTer18
NM_001127695.3:c.582dup NP_001121167.1:p.Pro195SerfsTer18
NM_001167594.3:c.531dup NP_001161066.2:p.Pro178SerfsTer18
NR_133656.2:n.627dup