Canonical Allele Identifier: CA2366420883
Gene: CTSA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45892038A= , CM000682.2:g.45892038A= GRCh38
NC_000020.10:g.44520677A= , CM000682.1:g.44520677A= GRCh37
NC_000020.9:g.43954084A= NCBI36
NG_008291.1:g.6087A=
NG_033108.1:g.4250T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000480961.3:n.723+11A=
ENST00000484855.4:n.356+11A=
ENST00000493522.8:n.334+11A=
ENST00000606066.3:n.723+11A=
ENST00000606782.3:n.193A=
ENST00000607187.3:n.723+11A=
ENST00000607212.3:n.517+11A=
ENST00000607814.7:n.494A=
ENST00000677755.2:n.418A=
ENST00000678622.2:n.723+11A=
ENST00000678691.2:n.723+11A=
ENST00000678988.2:n.1345+11A=
ENST00000679053.2:n.723+11A=
ENST00000679343.2:n.723+11A=
ENST00000684198.1:n.723+11A=
ENST00000372459.7:c.306+11A= ENSP00000361537.2:n.306+11A=
ENST00000372484.8:c.360+11A= ENSP00000361562.3:n.360+11A=
ENST00000419493.3:c.306+11A= ENSP00000408533.3:n.306+11A=
ENST00000480961.2:n.333+11A=
ENST00000484855.3:n.356+11A=
ENST00000493522.7:n.334+11A=
ENST00000606066.2:n.371+11A=
ENST00000606394.6:c.248+276A= ENSP00000475827.1:n.248+276A=
ENST00000606782.2:n.193A=
ENST00000607187.2:n.237+11A=
ENST00000607212.2:n.517+11A=
ENST00000607482.6:c.306+11A= ENSP00000475524.2:n.306+11A=
ENST00000607814.6:n.494A=
ENST00000646241.3:c.306+11A= MANE Select ENSP00000493613.2:n.306+11A=
ENST00000676526.1:c.360+11A= ENSP00000504209.1:n.360+11A=
ENST00000676597.1:c.306+11A= ENSP00000503904.1:n.306+11A=
ENST00000676657.1:c.306+11A= ENSP00000504158.1:n.306+11A=
ENST00000676967.1:c.306+11A= ENSP00000502866.1:n.306+11A=
ENST00000677394.1:c.360+11A= ENSP00000504790.1:n.360+11A=
ENST00000677525.1:c.*129+11A= ENSP00000504197.1:n.*129+11A=
ENST00000677755.1:n.418A=
ENST00000678025.1:c.306+11A= ENSP00000503463.1:n.306+11A=
ENST00000678078.1:c.360+11A= ENSP00000502993.1:n.360+11A=
ENST00000678217.1:c.306+11A= ENSP00000504109.1:n.306+11A=
ENST00000678331.1:c.306+11A= ENSP00000504524.1:n.306+11A=
ENST00000678443.1:c.306+11A= ENSP00000504006.1:n.306+11A=
ENST00000678512.1:n.496+11A=
ENST00000678622.1:n.351+11A=
ENST00000678691.1:n.184+11A=
ENST00000678939.1:c.306+11A= ENSP00000503404.1:n.306+11A=
ENST00000678988.1:n.1345+11A=
ENST00000679053.1:n.351+11A=
ENST00000679343.1:n.344+11A=
ENST00000191018.9:c.306+11A= ENSP00000191018.5:n.306+11A=
ENST00000354880.9:c.360+11A= ENSP00000346952.4:n.360+11A=
ENST00000372459.6:c.306+11A= ENSP00000361537.2:n.306+11A=
ENST00000372484.7:c.360+11A= ENSP00000361562.3:n.360+11A=
ENST00000606066.1:n.351+11A=
ENST00000606394.5:c.248+276A= ENSP00000475827.1:n.248+276A=
ENST00000606788.5:c.360+11A= ENSP00000476235.1:n.360+11A=
ENST00000607212.1:n.482+11A=
ENST00000607482.5:c.306+11A= ENSP00000475524.1:n.306+11A=
ENST00000607814.5:n.484+11A=
ENST00000607841.5:n.362A=
NM_000308.2:c.360+11A= NP_000299.2:n.360+11A=
NM_000308.3:c.360+11A= NP_000299.2:n.360+11A=
NM_001127695.1:c.306+11A= NP_001121167.1:n.306+11A=
NM_001127695.2:c.306+11A= NP_001121167.1:n.306+11A=
NM_001167594.1:c.360+11A= NP_001161066.1:n.360+11A=
NM_001167594.2:c.360+11A= NP_001161066.1:n.360+11A=
NR_133656.1:n.1542+11A=
NM_000308.4:c.306+11A= MANE Select NP_000299.3:n.306+11A=
NM_001127695.3:c.306+11A= NP_001121167.1:n.306+11A=
NM_001167594.3:c.306+11A= NP_001161066.2:n.306+11A=
NR_133656.2:n.351+11A=