Canonical Allele Identifier: CA2737032004
Gene: CTSA HGNC NCBI

Linked Data

dbSNP Id: rs2145813236

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.45891615_45891616insCCT , CM000682.2:g.45891615_45891616insCCT GRCh38
NC_000020.10:g.44520254_44520255insCCT , CM000682.1:g.44520254_44520255insCCT GRCh37
NC_000020.9:g.43953661_43953662insCCT NCBI36
NG_008291.1:g.5664_5665insCCT
NG_033108.1:g.4674_4675insGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000480961.3:n.464_465insCCT
ENST00000484855.4:n.97_98insCCT
ENST00000493522.8:n.75_76insCCT
ENST00000606066.3:n.464_465insCCT
ENST00000607187.3:n.464_465insCCT
ENST00000607212.3:n.105_106insCCT
ENST00000607814.7:n.71_72insCCT
ENST00000678622.2:n.464_465insCCT
ENST00000678691.2:n.464_465insCCT
ENST00000678988.2:n.1086_1087insCCT
ENST00000679053.2:n.464_465insCCT
ENST00000679343.2:n.464_465insCCT
ENST00000684198.1:n.464_465insCCT
ENST00000372459.7:c.47_48insCCT ENSP00000361537.2:p.Leu16_Leu17insLeu
ENST00000372484.8:c.101_102insCCT ENSP00000361562.3:p.Leu34_Leu35insLeu
ENST00000419493.3:c.47_48insCCT ENSP00000408533.3:p.Leu16_Leu17insLeu
ENST00000480961.2:n.74_75insCCT
ENST00000484855.3:n.97_98insCCT
ENST00000493522.7:n.75_76insCCT
ENST00000606066.2:n.112_113insCCT
ENST00000606394.6:c.101_102insCCT ENSP00000475827.1:p.Leu34_Leu35insLeu
ENST00000607212.2:n.105_106insCCT
ENST00000607482.6:c.47_48insCCT ENSP00000475524.2:p.Leu16_Leu17insLeu
ENST00000607814.6:n.71_72insCCT
ENST00000646241.3:c.47_48insCCT MANE Select ENSP00000493613.2:p.Leu16_Leu17insLeu
ENST00000676526.1:c.101_102insCCT ENSP00000504209.1:p.Leu34_Leu35insLeu
ENST00000676597.1:c.47_48insCCT ENSP00000503904.1:p.Leu16_Leu17insLeu
ENST00000676657.1:c.47_48insCCT ENSP00000504158.1:p.Leu16_Leu17insLeu
ENST00000676967.1:c.47_48insCCT ENSP00000502866.1:p.Leu16_Leu17insLeu
ENST00000677394.1:c.101_102insCCT ENSP00000504790.1:p.Leu34_Leu35insLeu
ENST00000677525.1:c.47_48insCCT ENSP00000504197.1:p.Leu16_Leu17insLeu
ENST00000678025.1:c.47_48insCCT ENSP00000503463.1:p.Leu16_Leu17insLeu
ENST00000678078.1:c.101_102insCCT ENSP00000502993.1:p.Leu34_Leu35insLeu
ENST00000678217.1:c.47_48insCCT ENSP00000504109.1:p.Leu16_Leu17insLeu
ENST00000678331.1:c.47_48insCCT ENSP00000504524.1:p.Leu16_Leu17insLeu
ENST00000678443.1:c.47_48insCCT ENSP00000504006.1:p.Leu16_Leu17insLeu
ENST00000678512.1:n.84_85insCCT
ENST00000678622.1:n.92_93insCCT
ENST00000678939.1:c.47_48insCCT ENSP00000503404.1:p.Leu16_Leu17insLeu
ENST00000678988.1:n.1086_1087insCCT
ENST00000679053.1:n.92_93insCCT
ENST00000679343.1:n.85_86insCCT
ENST00000191018.9:c.47_48insCCT ENSP00000191018.5:p.Leu16_Leu17insLeu
ENST00000354880.9:c.101_102insCCT ENSP00000346952.4:p.Leu34_Leu35insLeu
ENST00000372459.6:c.47_48insCCT ENSP00000361537.2:p.Leu16_Leu17insLeu
ENST00000372484.7:c.101_102insCCT ENSP00000361562.3:p.Leu34_Leu35insLeu
ENST00000606066.1:n.92_93insCCT
ENST00000606394.5:c.101_102insCCT ENSP00000475827.1:p.Leu34_Leu35insLeu
ENST00000606788.5:c.101_102insCCT ENSP00000476235.1:p.Leu34_Leu35insLeu
ENST00000607212.1:n.70_71insCCT
ENST00000607482.5:c.47_48insCCT ENSP00000475524.1:p.Leu16_Leu17insLeu
ENST00000607814.5:n.72_73insCCT
ENST00000607841.5:n.92_93insCCT
NM_000308.2:c.101_102insCCT NP_000299.2:p.Leu34_Leu35insLeu
NM_000308.3:c.101_102insCCT NP_000299.2:p.Leu34_Leu35insLeu
NM_001127695.1:c.47_48insCCT NP_001121167.1:p.Leu16_Leu17insLeu
NM_001127695.2:c.47_48insCCT NP_001121167.1:p.Leu16_Leu17insLeu
NM_001167594.1:c.101_102insCCT NP_001161066.1:p.Leu34_Leu35insLeu
NM_001167594.2:c.101_102insCCT NP_001161066.1:p.Leu34_Leu35insLeu
NR_133656.1:n.1283_1284insCCT
NM_000308.4:c.47_48insCCT MANE Select NP_000299.3:p.Leu16_Leu17insLeu
NM_001127695.3:c.47_48insCCT NP_001121167.1:p.Leu16_Leu17insLeu
NM_001167594.3:c.47_48insCCT NP_001161066.2:p.Leu16_Leu17insLeu
NR_133656.2:n.92_93insCCT