Canonical Allele Identifier: CA409249613

Gene: CTSA

Linked Data

• MyVariant Identifiers: chr20:g.44521494T>G (hg19) ; chr20:g.45892855T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45892855T>G , CM000682.2:g.45892855T>G	GRCh38
NC_000020.10:g.44521494T>G , CM000682.1:g.44521494T>G	GRCh37
NC_000020.9:g.43954901T>G	NCBI36
NG_008291.1:g.6904T>G
NG_033108.1:g.3433A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480961.3:n.992T>G
ENST00000484855.4:n.625T>G
ENST00000493522.8:n.603T>G
ENST00000606066.3:n.1066T>G
ENST00000606782.3:n.696T>G
ENST00000607187.3:n.992T>G
ENST00000607212.3:n.786T>G
ENST00000607814.7:n.1311T>G
ENST00000677755.2:n.995T>G
ENST00000678622.2:n.992T>G
ENST00000678691.2:n.992T>G
ENST00000678988.2:n.1614T>G
ENST00000679053.2:n.992T>G
ENST00000679343.2:n.992T>G
ENST00000684198.1:n.992T>G
ENST00000372459.7:c.575T>G	ENSP00000361537.2:p.Met192Arg
ENST00000372484.8:c.629T>G	ENSP00000361562.3:p.Met210Arg
ENST00000419493.3:c.575T>G	ENSP00000408533.3:p.Met192Arg
ENST00000480961.2:n.602T>G
ENST00000484855.3:n.625T>G
ENST00000493522.7:n.603T>G
ENST00000606066.2:n.714T>G
ENST00000606394.6:c.*217T>G	ENSP00000475827.1:n.*217T>G
ENST00000606782.2:n.696T>G
ENST00000607187.2:n.506T>G
ENST00000607212.2:n.786T>G
ENST00000607482.6:c.575T>G	ENSP00000475524.2:p.Met192Arg
ENST00000607814.6:n.1311T>G
ENST00000646241.3:c.575T>G MANE Select	ENSP00000493613.2:p.Met192Arg
ENST00000676526.1:c.629T>G	ENSP00000504209.1:p.Met210Arg
ENST00000676597.1:c.575T>G	ENSP00000503904.1:p.Met192Arg
ENST00000676657.1:c.575T>G	ENSP00000504158.1:p.Met192Arg
ENST00000676967.1:c.575T>G	ENSP00000502866.1:p.Met192Arg
ENST00000677394.1:c.629T>G	ENSP00000504790.1:p.Met210Arg
ENST00000677525.1:c.*398T>G	ENSP00000504197.1:n.*398T>G
ENST00000677755.1:n.995T>G
ENST00000678025.1:c.575T>G	ENSP00000503463.1:p.Met192Arg
ENST00000678078.1:c.629T>G	ENSP00000502993.1:p.Met210Arg
ENST00000678217.1:c.575T>G	ENSP00000504109.1:p.Met192Arg
ENST00000678331.1:c.575T>G	ENSP00000504524.1:p.Met192Arg
ENST00000678443.1:c.575T>G	ENSP00000504006.1:p.Met192Arg
ENST00000678512.1:n.839T>G
ENST00000678622.1:n.620T>G
ENST00000678691.1:n.453T>G
ENST00000678939.1:c.575T>G	ENSP00000503404.1:p.Met192Arg
ENST00000678988.1:n.1614T>G
ENST00000679053.1:n.620T>G
ENST00000679343.1:n.613T>G
ENST00000191018.9:c.575T>G	ENSP00000191018.5:p.Met192Arg
ENST00000354880.9:c.578T>G	ENSP00000346952.4:p.Met193Arg
ENST00000372459.6:c.575T>G	ENSP00000361537.2:p.Met192Arg
ENST00000372484.7:c.629T>G	ENSP00000361562.3:p.Met210Arg
ENST00000419493.2:c.104T>G	ENSP00000408533.2:p.Met35Arg
ENST00000485627.1:n.236T>G
ENST00000606394.5:c.*217T>G	ENSP00000475827.1:n.*217T>G
ENST00000606782.1:n.208T>G
ENST00000606788.5:c.629T>G	ENSP00000476235.1:p.Met210Arg
NM_000308.2:c.629T>G	NP_000299.2:p.Met210Arg
NM_000308.3:c.629T>G	NP_000299.2:p.Met210Arg
NM_001127695.1:c.575T>G	NP_001121167.1:p.Met192Arg
NM_001127695.2:c.575T>G	NP_001121167.1:p.Met192Arg
NM_001167594.1:c.578T>G	NP_001161066.1:p.Met193Arg
NM_001167594.2:c.578T>G	NP_001161066.1:p.Met193Arg
NR_133656.1:n.1811T>G
NM_000308.4:c.575T>G MANE Select	NP_000299.3:p.Met192Arg
NM_001127695.3:c.575T>G	NP_001121167.1:p.Met192Arg
NM_001167594.3:c.524T>G	NP_001161066.2:p.Met175Arg
NR_133656.2:n.620T>G