Canonical Allele Identifier: CA2366423572
Gene: CTSA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45898076G= , CM000682.2:g.45898076G= GRCh38
NC_000020.10:g.44526715G= , CM000682.1:g.44526715G= GRCh37
NC_000020.9:g.43960122G= NCBI36
NG_008291.1:g.12125G=
NG_012115.1:g.19072C=
NG_012115.2:g.19072C=

Transcript Alleles

HGVS Amino-acid change
ENST00000480961.3:n.5463G=
ENST00000484855.4:n.4081G=
ENST00000493522.8:n.1693G=
ENST00000606066.3:n.1817G=
ENST00000606782.3:n.1447G=
ENST00000607187.3:n.4250G=
ENST00000607212.3:n.1537G=
ENST00000607814.7:n.3077G=
ENST00000677755.2:n.1746G=
ENST00000678622.2:n.2617G=
ENST00000678691.2:n.3574G=
ENST00000678988.2:n.2704G=
ENST00000679053.2:n.4448G=
ENST00000679343.2:n.4787G=
ENST00000684198.1:n.1941G=
ENST00000372459.7:c.1326G= ENSP00000361537.2:p.Lys442=
ENST00000372484.8:c.1380G= ENSP00000361562.3:p.Lys460=
ENST00000484855.3:n.4081G=
ENST00000493522.7:n.1693G=
ENST00000606066.2:n.1465G=
ENST00000607187.2:n.3764G=
ENST00000607212.2:n.1537G=
ENST00000607482.6:c.1326G= ENSP00000475524.2:p.Lys442=
ENST00000646241.3:c.1326G= MANE Select ENSP00000493613.2:p.Lys442=
ENST00000676597.1:c.1165G= ENSP00000503904.1:n.1165G=
ENST00000676967.1:c.*719G= ENSP00000502866.1:n.*719G=
ENST00000677394.1:c.1380G= ENSP00000504790.1:p.Lys460=
ENST00000677525.1:c.*1149G= ENSP00000504197.1:n.*1149G=
ENST00000677755.1:n.1746G=
ENST00000678025.1:c.*1390G= ENSP00000503463.1:n.*1390G=
ENST00000678078.1:c.*889G= ENSP00000502993.1:n.*889G=
ENST00000678217.1:c.2108G= ENSP00000504109.1:n.2108G=
ENST00000678331.1:c.*44G= ENSP00000504524.1:n.*44G=
ENST00000678443.1:c.1236G= ENSP00000504006.1:p.Lys412=
ENST00000678512.1:n.5887G=
ENST00000678622.1:n.2245G=
ENST00000678691.1:n.3035G=
ENST00000678939.1:c.*665G= ENSP00000503404.1:n.*665G=
ENST00000678988.1:n.2704G=
ENST00000679053.1:n.4076G=
ENST00000679343.1:n.4408G=
ENST00000191018.9:c.1326G= ENSP00000191018.5:p.Lys442=
ENST00000354880.9:c.1329G= ENSP00000346952.4:p.Lys443=
ENST00000372459.6:c.1326G= ENSP00000361537.2:p.Lys442=
ENST00000372484.7:c.1380G= ENSP00000361562.3:p.Lys460=
ENST00000484855.2:n.1696G=
ENST00000606000.1:n.350G=
ENST00000606788.5:c.*691G= ENSP00000476235.1:n.*691G=
NM_000308.2:c.1380G= NP_000299.2:p.Lys460=
NM_000308.3:c.1380G= NP_000299.2:p.Lys460=
NM_001127695.1:c.1326G= NP_001121167.1:p.Lys442=
NM_001127695.2:c.1326G= NP_001121167.1:p.Lys442=
NM_001167594.1:c.1329G= NP_001161066.1:p.Lys443=
NM_001167594.2:c.1329G= NP_001161066.1:p.Lys443=
NR_133656.1:n.2569G=
NM_000308.4:c.1326G= MANE Select NP_000299.3:p.Lys442=
NM_001127695.3:c.1326G= NP_001121167.1:p.Lys442=
NM_001167594.3:c.1275G= NP_001161066.2:p.Lys425=
NR_133656.2:n.1378G=