Canonical Allele Identifier: CA2366420767

Gene: CTSA

Linked Data

• dbSNP Id: rs1986963408

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45891797_45891798del , CM000682.2:g.45891797_45891798del	GRCh38
NC_000020.10:g.44520436_44520437del , CM000682.1:g.44520436_44520437del	GRCh37
NC_000020.9:g.43953843_43953844del	NCBI36
NG_008291.1:g.5846_5847del
NG_033108.1:g.4490_4491del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480961.3:n.611+35_611+36del
ENST00000484855.4:n.244+35_244+36del
ENST00000493522.8:n.222+35_222+36del
ENST00000606066.3:n.611+35_611+36del
ENST00000607187.3:n.611+35_611+36del
ENST00000607212.3:n.287_288del
ENST00000607814.7:n.253_254del
ENST00000677755.2:n.177_178del
ENST00000678622.2:n.611+35_611+36del
ENST00000678691.2:n.611+35_611+36del
ENST00000678988.2:n.1233+35_1233+36del
ENST00000679053.2:n.611+35_611+36del
ENST00000679343.2:n.611+35_611+36del
ENST00000684198.1:n.611+35_611+36del
ENST00000372459.7:c.194+35_194+36del	ENSP00000361537.2:n.194+35_194+36del
ENST00000372484.8:c.248+35_248+36del	ENSP00000361562.3:n.248+35_248+36del
ENST00000419493.3:c.194+35_194+36del	ENSP00000408533.3:n.194+35_194+36del
ENST00000480961.2:n.221+35_221+36del
ENST00000484855.3:n.244+35_244+36del
ENST00000493522.7:n.222+35_222+36del
ENST00000606066.2:n.259+35_259+36del
ENST00000606394.6:c.248+35_248+36del	ENSP00000475827.1:n.248+35_248+36del
ENST00000607187.2:n.125+35_125+36del
ENST00000607212.2:n.287_288del
ENST00000607482.6:c.194+35_194+36del	ENSP00000475524.2:n.194+35_194+36del
ENST00000607814.6:n.253_254del
ENST00000646241.3:c.194+35_194+36del MANE Select	ENSP00000493613.2:n.194+35_194+36del
ENST00000676526.1:c.248+35_248+36del	ENSP00000504209.1:n.248+35_248+36del
ENST00000676597.1:c.194+35_194+36del	ENSP00000503904.1:n.194+35_194+36del
ENST00000676657.1:c.194+35_194+36del	ENSP00000504158.1:n.194+35_194+36del
ENST00000676967.1:c.194+35_194+36del	ENSP00000502866.1:n.194+35_194+36del
ENST00000677394.1:c.248+35_248+36del	ENSP00000504790.1:n.248+35_248+36del
ENST00000677525.1:c.229_230del	ENSP00000504197.1:p.Lys77GlufsTer?
ENST00000677755.1:n.177_178del
ENST00000678025.1:c.194+35_194+36del	ENSP00000503463.1:n.194+35_194+36del
ENST00000678078.1:c.248+35_248+36del	ENSP00000502993.1:n.248+35_248+36del
ENST00000678217.1:c.194+35_194+36del	ENSP00000504109.1:n.194+35_194+36del
ENST00000678331.1:c.194+35_194+36del	ENSP00000504524.1:n.194+35_194+36del
ENST00000678443.1:c.194+35_194+36del	ENSP00000504006.1:n.194+35_194+36del
ENST00000678512.1:n.266_267del
ENST00000678622.1:n.239+35_239+36del
ENST00000678691.1:n.72+35_72+36del
ENST00000678939.1:c.194+35_194+36del	ENSP00000503404.1:n.194+35_194+36del
ENST00000678988.1:n.1233+35_1233+36del
ENST00000679053.1:n.239+35_239+36del
ENST00000679343.1:n.232+35_232+36del
ENST00000191018.9:c.194+35_194+36del	ENSP00000191018.5:n.194+35_194+36del
ENST00000354880.9:c.248+35_248+36del	ENSP00000346952.4:n.248+35_248+36del
ENST00000372459.6:c.194+35_194+36del	ENSP00000361537.2:n.194+35_194+36del
ENST00000372484.7:c.248+35_248+36del	ENSP00000361562.3:n.248+35_248+36del
ENST00000606066.1:n.239+35_239+36del
ENST00000606394.5:c.248+35_248+36del	ENSP00000475827.1:n.248+35_248+36del
ENST00000606788.5:c.248+35_248+36del	ENSP00000476235.1:n.248+35_248+36del
ENST00000607212.1:n.252_253del
ENST00000607482.5:c.194+35_194+36del	ENSP00000475524.1:n.194+35_194+36del
ENST00000607814.5:n.254_255del
ENST00000607841.5:n.239+35_239+36del
NM_000308.2:c.248+35_248+36del	NP_000299.2:n.248+35_248+36del
NM_000308.3:c.248+35_248+36del	NP_000299.2:n.248+35_248+36del
NM_001127695.1:c.194+35_194+36del	NP_001121167.1:n.194+35_194+36del
NM_001127695.2:c.194+35_194+36del	NP_001121167.1:n.194+35_194+36del
NM_001167594.1:c.248+35_248+36del	NP_001161066.1:n.248+35_248+36del
NM_001167594.2:c.248+35_248+36del	NP_001161066.1:n.248+35_248+36del
NR_133656.1:n.1430+35_1430+36del
NM_000308.4:c.194+35_194+36del MANE Select	NP_000299.3:n.194+35_194+36del
NM_001127695.3:c.194+35_194+36del	NP_001121167.1:n.194+35_194+36del
NM_001167594.3:c.194+35_194+36del	NP_001161066.2:n.194+35_194+36del
NR_133656.2:n.239+35_239+36del