Canonical Allele Identifier: CA2816512232

Gene: CTSA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45891767_45891768insTGGAGT , CM000682.2:g.45891767_45891768insTGGAGT	GRCh38
NC_000020.10:g.44520406_44520407insTGGAGT , CM000682.1:g.44520406_44520407insTGGAGT	GRCh37
NC_000020.9:g.43953813_43953814insTGGAGT	NCBI36
NG_008291.1:g.5816_5817insTGGAGT
NG_033108.1:g.4520_4521insACTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480961.3:n.611+5_611+6insTGGAGT
ENST00000484855.4:n.244+5_244+6insTGGAGT
ENST00000493522.8:n.222+5_222+6insTGGAGT
ENST00000606066.3:n.611+5_611+6insTGGAGT
ENST00000607187.3:n.611+5_611+6insTGGAGT
ENST00000607212.3:n.257_258insTGGAGT
ENST00000607814.7:n.223_224insTGGAGT
ENST00000677755.2:n.147_148insTGGAGT
ENST00000678622.2:n.611+5_611+6insTGGAGT
ENST00000678691.2:n.611+5_611+6insTGGAGT
ENST00000678988.2:n.1233+5_1233+6insTGGAGT
ENST00000679053.2:n.611+5_611+6insTGGAGT
ENST00000679343.2:n.611+5_611+6insTGGAGT
ENST00000684198.1:n.611+5_611+6insTGGAGT
ENST00000372459.7:c.194+5_194+6insTGGAGT	ENSP00000361537.2:n.194+5_194+6insTGGAGT
ENST00000372484.8:c.248+5_248+6insTGGAGT	ENSP00000361562.3:n.248+5_248+6insTGGAGT
ENST00000419493.3:c.194+5_194+6insTGGAGT	ENSP00000408533.3:n.194+5_194+6insTGGAGT
ENST00000480961.2:n.221+5_221+6insTGGAGT
ENST00000484855.3:n.244+5_244+6insTGGAGT
ENST00000493522.7:n.222+5_222+6insTGGAGT
ENST00000606066.2:n.259+5_259+6insTGGAGT
ENST00000606394.6:c.248+5_248+6insTGGAGT	ENSP00000475827.1:n.248+5_248+6insTGGAGT
ENST00000607187.2:n.125+5_125+6insTGGAGT
ENST00000607212.2:n.257_258insTGGAGT
ENST00000607482.6:c.194+5_194+6insTGGAGT	ENSP00000475524.2:n.194+5_194+6insTGGAGT
ENST00000607814.6:n.223_224insTGGAGT
ENST00000646241.3:c.194+5_194+6insTGGAGT MANE Select	ENSP00000493613.2:n.194+5_194+6insTGGAGT
ENST00000676526.1:c.248+5_248+6insTGGAGT	ENSP00000504209.1:n.248+5_248+6insTGGAGT
ENST00000676597.1:c.194+5_194+6insTGGAGT	ENSP00000503904.1:n.194+5_194+6insTGGAGT
ENST00000676657.1:c.194+5_194+6insTGGAGT	ENSP00000504158.1:n.194+5_194+6insTGGAGT
ENST00000676967.1:c.194+5_194+6insTGGAGT	ENSP00000502866.1:n.194+5_194+6insTGGAGT
ENST00000677394.1:c.248+5_248+6insTGGAGT	ENSP00000504790.1:n.248+5_248+6insTGGAGT
ENST00000677525.1:c.199_200insTGGAGT	ENSP00000504197.1:p.Ala67delinsValGluSer
ENST00000677755.1:n.147_148insTGGAGT
ENST00000678025.1:c.194+5_194+6insTGGAGT	ENSP00000503463.1:n.194+5_194+6insTGGAGT
ENST00000678078.1:c.248+5_248+6insTGGAGT	ENSP00000502993.1:n.248+5_248+6insTGGAGT
ENST00000678217.1:c.194+5_194+6insTGGAGT	ENSP00000504109.1:n.194+5_194+6insTGGAGT
ENST00000678331.1:c.194+5_194+6insTGGAGT	ENSP00000504524.1:n.194+5_194+6insTGGAGT
ENST00000678443.1:c.194+5_194+6insTGGAGT	ENSP00000504006.1:n.194+5_194+6insTGGAGT
ENST00000678512.1:n.236_237insTGGAGT
ENST00000678622.1:n.239+5_239+6insTGGAGT
ENST00000678691.1:n.72+5_72+6insTGGAGT
ENST00000678939.1:c.194+5_194+6insTGGAGT	ENSP00000503404.1:n.194+5_194+6insTGGAGT
ENST00000678988.1:n.1233+5_1233+6insTGGAGT
ENST00000679053.1:n.239+5_239+6insTGGAGT
ENST00000679343.1:n.232+5_232+6insTGGAGT
ENST00000191018.9:c.194+5_194+6insTGGAGT	ENSP00000191018.5:n.194+5_194+6insTGGAGT
ENST00000354880.9:c.248+5_248+6insTGGAGT	ENSP00000346952.4:n.248+5_248+6insTGGAGT
ENST00000372459.6:c.194+5_194+6insTGGAGT	ENSP00000361537.2:n.194+5_194+6insTGGAGT
ENST00000372484.7:c.248+5_248+6insTGGAGT	ENSP00000361562.3:n.248+5_248+6insTGGAGT
ENST00000606066.1:n.239+5_239+6insTGGAGT
ENST00000606394.5:c.248+5_248+6insTGGAGT	ENSP00000475827.1:n.248+5_248+6insTGGAGT
ENST00000606788.5:c.248+5_248+6insTGGAGT	ENSP00000476235.1:n.248+5_248+6insTGGAGT
ENST00000607212.1:n.222_223insTGGAGT
ENST00000607482.5:c.194+5_194+6insTGGAGT	ENSP00000475524.1:n.194+5_194+6insTGGAGT
ENST00000607814.5:n.224_225insTGGAGT
ENST00000607841.5:n.239+5_239+6insTGGAGT
NM_000308.2:c.248+5_248+6insTGGAGT	NP_000299.2:n.248+5_248+6insTGGAGT
NM_000308.3:c.248+5_248+6insTGGAGT	NP_000299.2:n.248+5_248+6insTGGAGT
NM_001127695.1:c.194+5_194+6insTGGAGT	NP_001121167.1:n.194+5_194+6insTGGAGT
NM_001127695.2:c.194+5_194+6insTGGAGT	NP_001121167.1:n.194+5_194+6insTGGAGT
NM_001167594.1:c.248+5_248+6insTGGAGT	NP_001161066.1:n.248+5_248+6insTGGAGT
NM_001167594.2:c.248+5_248+6insTGGAGT	NP_001161066.1:n.248+5_248+6insTGGAGT
NR_133656.1:n.1430+5_1430+6insTGGAGT
NM_000308.4:c.194+5_194+6insTGGAGT MANE Select	NP_000299.3:n.194+5_194+6insTGGAGT
NM_001127695.3:c.194+5_194+6insTGGAGT	NP_001121167.1:n.194+5_194+6insTGGAGT
NM_001167594.3:c.194+5_194+6insTGGAGT	NP_001161066.2:n.194+5_194+6insTGGAGT
NR_133656.2:n.239+5_239+6insTGGAGT