Canonical Allele Identifier: CA409248687

Gene: CTSA

Linked Data

• MyVariant Identifiers: chr20:g.44520652C>G (hg19) ; chr20:g.45892013C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45892013C>G , CM000682.2:g.45892013C>G	GRCh38
NC_000020.10:g.44520652C>G , CM000682.1:g.44520652C>G	GRCh37
NC_000020.9:g.43954059C>G	NCBI36
NG_008291.1:g.6062C>G
NG_033108.1:g.4275G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480961.3:n.709C>G
ENST00000484855.4:n.342C>G
ENST00000493522.8:n.320C>G
ENST00000606066.3:n.709C>G
ENST00000606782.3:n.168C>G
ENST00000607187.3:n.709C>G
ENST00000607212.3:n.503C>G
ENST00000607814.7:n.469C>G
ENST00000677755.2:n.393C>G
ENST00000678622.2:n.709C>G
ENST00000678691.2:n.709C>G
ENST00000678988.2:n.1331C>G
ENST00000679053.2:n.709C>G
ENST00000679343.2:n.709C>G
ENST00000684198.1:n.709C>G
ENST00000372459.7:c.292C>G	ENSP00000361537.2:p.His98Asp
ENST00000372484.8:c.346C>G	ENSP00000361562.3:p.His116Asp
ENST00000419493.3:c.292C>G	ENSP00000408533.3:p.His98Asp
ENST00000480961.2:n.319C>G
ENST00000484855.3:n.342C>G
ENST00000493522.7:n.320C>G
ENST00000606066.2:n.357C>G
ENST00000606394.6:c.248+251C>G	ENSP00000475827.1:n.248+251C>G
ENST00000606782.2:n.168C>G
ENST00000607187.2:n.223C>G
ENST00000607212.2:n.503C>G
ENST00000607482.6:c.292C>G	ENSP00000475524.2:p.His98Asp
ENST00000607814.6:n.469C>G
ENST00000646241.3:c.292C>G MANE Select	ENSP00000493613.2:p.His98Asp
ENST00000676526.1:c.346C>G	ENSP00000504209.1:p.His116Asp
ENST00000676597.1:c.292C>G	ENSP00000503904.1:p.His98Asp
ENST00000676657.1:c.292C>G	ENSP00000504158.1:p.His98Asp
ENST00000676967.1:c.292C>G	ENSP00000502866.1:p.His98Asp
ENST00000677394.1:c.346C>G	ENSP00000504790.1:p.His116Asp
ENST00000677525.1:c.*115C>G	ENSP00000504197.1:n.*115C>G
ENST00000677755.1:n.393C>G
ENST00000678025.1:c.292C>G	ENSP00000503463.1:p.His98Asp
ENST00000678078.1:c.346C>G	ENSP00000502993.1:p.His116Asp
ENST00000678217.1:c.292C>G	ENSP00000504109.1:p.His98Asp
ENST00000678331.1:c.292C>G	ENSP00000504524.1:p.His98Asp
ENST00000678443.1:c.292C>G	ENSP00000504006.1:p.His98Asp
ENST00000678512.1:n.482C>G
ENST00000678622.1:n.337C>G
ENST00000678691.1:n.170C>G
ENST00000678939.1:c.292C>G	ENSP00000503404.1:p.His98Asp
ENST00000678988.1:n.1331C>G
ENST00000679053.1:n.337C>G
ENST00000679343.1:n.330C>G
ENST00000191018.9:c.292C>G	ENSP00000191018.5:p.His98Asp
ENST00000354880.9:c.346C>G	ENSP00000346952.4:p.His116Asp
ENST00000372459.6:c.292C>G	ENSP00000361537.2:p.His98Asp
ENST00000372484.7:c.346C>G	ENSP00000361562.3:p.His116Asp
ENST00000606066.1:n.337C>G
ENST00000606394.5:c.248+251C>G	ENSP00000475827.1:n.248+251C>G
ENST00000606788.5:c.346C>G	ENSP00000476235.1:p.His116Asp
ENST00000607212.1:n.468C>G
ENST00000607482.5:c.292C>G	ENSP00000475524.1:p.His98Asp
ENST00000607814.5:n.470C>G
ENST00000607841.5:n.337C>G
NM_000308.2:c.346C>G	NP_000299.2:p.His116Asp
NM_000308.3:c.346C>G	NP_000299.2:p.His116Asp
NM_001127695.1:c.292C>G	NP_001121167.1:p.His98Asp
NM_001127695.2:c.292C>G	NP_001121167.1:p.His98Asp
NM_001167594.1:c.346C>G	NP_001161066.1:p.His116Asp
NM_001167594.2:c.346C>G	NP_001161066.1:p.His116Asp
NR_133656.1:n.1528C>G
NM_000308.4:c.292C>G MANE Select	NP_000299.3:p.His98Asp
NM_001127695.3:c.292C>G	NP_001121167.1:p.His98Asp
NM_001167594.3:c.292C>G	NP_001161066.2:p.His98Asp
NR_133656.2:n.337C>G