Canonical Allele Identifier: CA2366423567

Gene: CTSA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45898065G= , CM000682.2:g.45898065G=	GRCh38
NC_000020.10:g.44526704G= , CM000682.1:g.44526704G=	GRCh37
NC_000020.9:g.43960111G=	NCBI36
NG_008291.1:g.12114G=
NG_012115.1:g.19083C=
NG_012115.2:g.19083C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480961.3:n.5452G=
ENST00000484855.4:n.4070G=
ENST00000493522.8:n.1682G=
ENST00000606066.3:n.1806G=
ENST00000606782.3:n.1436G=
ENST00000607187.3:n.4239G=
ENST00000607212.3:n.1526G=
ENST00000607814.7:n.3066G=
ENST00000677755.2:n.1735G=
ENST00000678622.2:n.2606G=
ENST00000678691.2:n.3563G=
ENST00000678988.2:n.2693G=
ENST00000679053.2:n.4437G=
ENST00000679343.2:n.4776G=
ENST00000684198.1:n.1930G=
ENST00000372459.7:c.1315G=	ENSP00000361537.2:p.Gly439=
ENST00000372484.8:c.1369G=	ENSP00000361562.3:p.Gly457=
ENST00000484855.3:n.4070G=
ENST00000493522.7:n.1682G=
ENST00000606066.2:n.1454G=
ENST00000607187.2:n.3753G=
ENST00000607212.2:n.1526G=
ENST00000607482.6:c.1315G=	ENSP00000475524.2:p.Gly439=
ENST00000646241.3:c.1315G= MANE Select	ENSP00000493613.2:p.Gly439=
ENST00000676597.1:c.1154G=	ENSP00000503904.1:n.1154G=
ENST00000676967.1:c.*708G=	ENSP00000502866.1:n.*708G=
ENST00000677394.1:c.1369G=	ENSP00000504790.1:p.Gly457=
ENST00000677525.1:c.*1138G=	ENSP00000504197.1:n.*1138G=
ENST00000677755.1:n.1735G=
ENST00000678025.1:c.*1379G=	ENSP00000503463.1:n.*1379G=
ENST00000678078.1:c.*878G=	ENSP00000502993.1:n.*878G=
ENST00000678217.1:c.2097G=	ENSP00000504109.1:n.2097G=
ENST00000678331.1:c.*33G=	ENSP00000504524.1:n.*33G=
ENST00000678443.1:c.1225G=	ENSP00000504006.1:p.Gly409=
ENST00000678512.1:n.5876G=
ENST00000678622.1:n.2234G=
ENST00000678691.1:n.3024G=
ENST00000678939.1:c.*654G=	ENSP00000503404.1:n.*654G=
ENST00000678988.1:n.2693G=
ENST00000679053.1:n.4065G=
ENST00000679343.1:n.4397G=
ENST00000191018.9:c.1315G=	ENSP00000191018.5:p.Gly439=
ENST00000354880.9:c.1318G=	ENSP00000346952.4:p.Gly440=
ENST00000372459.6:c.1315G=	ENSP00000361537.2:p.Gly439=
ENST00000372484.7:c.1369G=	ENSP00000361562.3:p.Gly457=
ENST00000484855.2:n.1685G=
ENST00000606000.1:n.339G=
ENST00000606788.5:c.*680G=	ENSP00000476235.1:n.*680G=
NM_000308.2:c.1369G=	NP_000299.2:p.Gly457=
NM_000308.3:c.1369G=	NP_000299.2:p.Gly457=
NM_001127695.1:c.1315G=	NP_001121167.1:p.Gly439=
NM_001127695.2:c.1315G=	NP_001121167.1:p.Gly439=
NM_001167594.1:c.1318G=	NP_001161066.1:p.Gly440=
NM_001167594.2:c.1318G=	NP_001161066.1:p.Gly440=
NR_133656.1:n.2558G=
NM_000308.4:c.1315G= MANE Select	NP_000299.3:p.Gly439=
NM_001127695.3:c.1315G=	NP_001121167.1:p.Gly439=
NM_001167594.3:c.1264G=	NP_001161066.2:p.Gly422=
NR_133656.2:n.1367G=