Canonical Allele Identifier: CA2366421238

Gene: CTSA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45892849T= , CM000682.2:g.45892849T=	GRCh38
NC_000020.10:g.44521488T= , CM000682.1:g.44521488T=	GRCh37
NC_000020.9:g.43954895T=	NCBI36
NG_008291.1:g.6898T=
NG_033108.1:g.3439A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480961.3:n.986T=
ENST00000484855.4:n.619T=
ENST00000493522.8:n.597T=
ENST00000606066.3:n.1060T=
ENST00000606782.3:n.690T=
ENST00000607187.3:n.986T=
ENST00000607212.3:n.780T=
ENST00000607814.7:n.1305T=
ENST00000677755.2:n.989T=
ENST00000678622.2:n.986T=
ENST00000678691.2:n.986T=
ENST00000678988.2:n.1608T=
ENST00000679053.2:n.986T=
ENST00000679343.2:n.986T=
ENST00000684198.1:n.986T=
ENST00000372459.7:c.569T=	ENSP00000361537.2:p.Leu190=
ENST00000372484.8:c.623T=	ENSP00000361562.3:p.Leu208=
ENST00000419493.3:c.569T=	ENSP00000408533.3:p.Leu190=
ENST00000480961.2:n.596T=
ENST00000484855.3:n.619T=
ENST00000493522.7:n.597T=
ENST00000606066.2:n.708T=
ENST00000606394.6:c.*211T=	ENSP00000475827.1:n.*211T=
ENST00000606782.2:n.690T=
ENST00000607187.2:n.500T=
ENST00000607212.2:n.780T=
ENST00000607482.6:c.569T=	ENSP00000475524.2:p.Leu190=
ENST00000607814.6:n.1305T=
ENST00000646241.3:c.569T= MANE Select	ENSP00000493613.2:p.Leu190=
ENST00000676526.1:c.623T=	ENSP00000504209.1:p.Leu208=
ENST00000676597.1:c.569T=	ENSP00000503904.1:p.Leu190=
ENST00000676657.1:c.569T=	ENSP00000504158.1:p.Leu190=
ENST00000676967.1:c.569T=	ENSP00000502866.1:p.Leu190=
ENST00000677394.1:c.623T=	ENSP00000504790.1:p.Leu208=
ENST00000677525.1:c.*392T=	ENSP00000504197.1:n.*392T=
ENST00000677755.1:n.989T=
ENST00000678025.1:c.569T=	ENSP00000503463.1:p.Leu190=
ENST00000678078.1:c.623T=	ENSP00000502993.1:p.Leu208=
ENST00000678217.1:c.569T=	ENSP00000504109.1:p.Leu190=
ENST00000678331.1:c.569T=	ENSP00000504524.1:p.Leu190=
ENST00000678443.1:c.569T=	ENSP00000504006.1:p.Leu190=
ENST00000678512.1:n.833T=
ENST00000678622.1:n.614T=
ENST00000678691.1:n.447T=
ENST00000678939.1:c.569T=	ENSP00000503404.1:p.Leu190=
ENST00000678988.1:n.1608T=
ENST00000679053.1:n.614T=
ENST00000679343.1:n.607T=
ENST00000191018.9:c.569T=	ENSP00000191018.5:p.Leu190=
ENST00000354880.9:c.572T=	ENSP00000346952.4:p.Leu191=
ENST00000372459.6:c.569T=	ENSP00000361537.2:p.Leu190=
ENST00000372484.7:c.623T=	ENSP00000361562.3:p.Leu208=
ENST00000419493.2:c.98T=	ENSP00000408533.2:p.Leu33=
ENST00000485627.1:n.230T=
ENST00000606394.5:c.*211T=	ENSP00000475827.1:n.*211T=
ENST00000606782.1:n.202T=
ENST00000606788.5:c.623T=	ENSP00000476235.1:p.Leu208=
NM_000308.2:c.623T=	NP_000299.2:p.Leu208=
NM_000308.3:c.623T=	NP_000299.2:p.Leu208=
NM_001127695.1:c.569T=	NP_001121167.1:p.Leu190=
NM_001127695.2:c.569T=	NP_001121167.1:p.Leu190=
NM_001167594.1:c.572T=	NP_001161066.1:p.Leu191=
NM_001167594.2:c.572T=	NP_001161066.1:p.Leu191=
NR_133656.1:n.1805T=
NM_000308.4:c.569T= MANE Select	NP_000299.3:p.Leu190=
NM_001127695.3:c.569T=	NP_001121167.1:p.Leu190=
NM_001167594.3:c.518T=	NP_001161066.2:p.Leu173=
NR_133656.2:n.614T=