Canonical Allele Identifier: CA409249146

Gene: CTSA

Linked Data

• COSMIC: COSM5034848
• MyVariant Identifiers: chr20:g.44521403C>A (hg19) ; chr20:g.45892764C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45892764C>A , CM000682.2:g.45892764C>A	GRCh38
NC_000020.10:g.44521403C>A , CM000682.1:g.44521403C>A	GRCh37
NC_000020.9:g.43954810C>A	NCBI36
NG_008291.1:g.6813C>A
NG_033108.1:g.3524G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480961.3:n.901C>A
ENST00000484855.4:n.534C>A
ENST00000493522.8:n.512C>A
ENST00000606066.3:n.975C>A
ENST00000606782.3:n.605C>A
ENST00000607187.3:n.901C>A
ENST00000607212.3:n.695C>A
ENST00000607814.7:n.1220C>A
ENST00000677755.2:n.904C>A
ENST00000678622.2:n.901C>A
ENST00000678691.2:n.901C>A
ENST00000678988.2:n.1523C>A
ENST00000679053.2:n.901C>A
ENST00000679343.2:n.901C>A
ENST00000684198.1:n.901C>A
ENST00000372459.7:c.484C>A	ENSP00000361537.2:p.Arg162Ser
ENST00000372484.8:c.538C>A	ENSP00000361562.3:p.Arg180Ser
ENST00000419493.3:c.484C>A	ENSP00000408533.3:p.Arg162Ser
ENST00000480961.2:n.511C>A
ENST00000484855.3:n.534C>A
ENST00000493522.7:n.512C>A
ENST00000606066.2:n.623C>A
ENST00000606394.6:c.*126C>A	ENSP00000475827.1:n.*126C>A
ENST00000606782.2:n.605C>A
ENST00000607187.2:n.415C>A
ENST00000607212.2:n.695C>A
ENST00000607482.6:c.484C>A	ENSP00000475524.2:p.Arg162Ser
ENST00000607814.6:n.1220C>A
ENST00000646241.3:c.484C>A MANE Select	ENSP00000493613.2:p.Arg162Ser
ENST00000676526.1:c.538C>A	ENSP00000504209.1:p.Arg180Ser
ENST00000676597.1:c.484C>A	ENSP00000503904.1:p.Arg162Ser
ENST00000676657.1:c.484C>A	ENSP00000504158.1:p.Arg162Ser
ENST00000676967.1:c.484C>A	ENSP00000502866.1:p.Arg162Ser
ENST00000677394.1:c.538C>A	ENSP00000504790.1:p.Arg180Ser
ENST00000677525.1:c.*307C>A	ENSP00000504197.1:n.*307C>A
ENST00000677755.1:n.904C>A
ENST00000678025.1:c.484C>A	ENSP00000503463.1:p.Arg162Ser
ENST00000678078.1:c.538C>A	ENSP00000502993.1:p.Arg180Ser
ENST00000678217.1:c.484C>A	ENSP00000504109.1:p.Arg162Ser
ENST00000678331.1:c.484C>A	ENSP00000504524.1:p.Arg162Ser
ENST00000678443.1:c.484C>A	ENSP00000504006.1:p.Arg162Ser
ENST00000678512.1:n.748C>A
ENST00000678622.1:n.529C>A
ENST00000678691.1:n.362C>A
ENST00000678939.1:c.484C>A	ENSP00000503404.1:p.Arg162Ser
ENST00000678988.1:n.1523C>A
ENST00000679053.1:n.529C>A
ENST00000679343.1:n.522C>A
ENST00000191018.9:c.484C>A	ENSP00000191018.5:p.Arg162Ser
ENST00000354880.9:c.487C>A	ENSP00000346952.4:p.Arg163Ser
ENST00000372459.6:c.484C>A	ENSP00000361537.2:p.Arg162Ser
ENST00000372484.7:c.538C>A	ENSP00000361562.3:p.Arg180Ser
ENST00000419493.2:c.13C>A	ENSP00000408533.2:p.Arg5Ser
ENST00000485627.1:n.145C>A
ENST00000606066.1:n.603C>A
ENST00000606394.5:c.*126C>A	ENSP00000475827.1:n.*126C>A
ENST00000606782.1:n.117C>A
ENST00000606788.5:c.538C>A	ENSP00000476235.1:p.Arg180Ser
NM_000308.2:c.538C>A	NP_000299.2:p.Arg180Ser
NM_000308.3:c.538C>A	NP_000299.2:p.Arg180Ser
NM_001127695.1:c.484C>A	NP_001121167.1:p.Arg162Ser
NM_001127695.2:c.484C>A	NP_001121167.1:p.Arg162Ser
NM_001167594.1:c.487C>A	NP_001161066.1:p.Arg163Ser
NM_001167594.2:c.487C>A	NP_001161066.1:p.Arg163Ser
NR_133656.1:n.1720C>A
NM_000308.4:c.484C>A MANE Select	NP_000299.3:p.Arg162Ser
NM_001127695.3:c.484C>A	NP_001121167.1:p.Arg162Ser
NM_001167594.3:c.433C>A	NP_001161066.2:p.Arg145Ser
NR_133656.2:n.529C>A