Canonical Allele Identifier: CA409249649

Gene: CTSA

Linked Data

• MyVariant Identifiers: chr20:g.44521499G>T (hg19) ; chr20:g.45892860G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45892860G>T , CM000682.2:g.45892860G>T	GRCh38
NC_000020.10:g.44521499G>T , CM000682.1:g.44521499G>T	GRCh37
NC_000020.9:g.43954906G>T	NCBI36
NG_008291.1:g.6909G>T
NG_033108.1:g.3428C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480961.3:n.997G>T
ENST00000484855.4:n.630G>T
ENST00000493522.8:n.608G>T
ENST00000606066.3:n.1071G>T
ENST00000606782.3:n.701G>T
ENST00000607187.3:n.997G>T
ENST00000607212.3:n.791G>T
ENST00000607814.7:n.1316G>T
ENST00000677755.2:n.1000G>T
ENST00000678622.2:n.997G>T
ENST00000678691.2:n.997G>T
ENST00000678988.2:n.1619G>T
ENST00000679053.2:n.997G>T
ENST00000679343.2:n.997G>T
ENST00000684198.1:n.997G>T
ENST00000372459.7:c.580G>T	ENSP00000361537.2:p.Asp194Tyr
ENST00000372484.8:c.634G>T	ENSP00000361562.3:p.Asp212Tyr
ENST00000419493.3:c.580G>T	ENSP00000408533.3:p.Asp194Tyr
ENST00000480961.2:n.607G>T
ENST00000484855.3:n.630G>T
ENST00000493522.7:n.608G>T
ENST00000606066.2:n.719G>T
ENST00000606394.6:c.*222G>T	ENSP00000475827.1:n.*222G>T
ENST00000606782.2:n.701G>T
ENST00000607187.2:n.511G>T
ENST00000607212.2:n.791G>T
ENST00000607482.6:c.580G>T	ENSP00000475524.2:p.Asp194Tyr
ENST00000607814.6:n.1316G>T
ENST00000646241.3:c.580G>T MANE Select	ENSP00000493613.2:p.Asp194Tyr
ENST00000676526.1:c.634G>T	ENSP00000504209.1:p.Asp212Tyr
ENST00000676597.1:c.580G>T	ENSP00000503904.1:p.Asp194Tyr
ENST00000676657.1:c.580G>T	ENSP00000504158.1:p.Asp194Tyr
ENST00000676967.1:c.580G>T	ENSP00000502866.1:p.Asp194Tyr
ENST00000677394.1:c.634G>T	ENSP00000504790.1:p.Asp212Tyr
ENST00000677525.1:c.*403G>T	ENSP00000504197.1:n.*403G>T
ENST00000677755.1:n.1000G>T
ENST00000678025.1:c.580G>T	ENSP00000503463.1:p.Asp194Tyr
ENST00000678078.1:c.634G>T	ENSP00000502993.1:p.Asp212Tyr
ENST00000678217.1:c.580G>T	ENSP00000504109.1:p.Asp194Tyr
ENST00000678331.1:c.580G>T	ENSP00000504524.1:p.Asp194Tyr
ENST00000678443.1:c.580G>T	ENSP00000504006.1:p.Asp194Tyr
ENST00000678512.1:n.844G>T
ENST00000678622.1:n.625G>T
ENST00000678691.1:n.458G>T
ENST00000678939.1:c.580G>T	ENSP00000503404.1:p.Asp194Tyr
ENST00000678988.1:n.1619G>T
ENST00000679053.1:n.625G>T
ENST00000679343.1:n.618G>T
ENST00000191018.9:c.580G>T	ENSP00000191018.5:p.Asp194Tyr
ENST00000354880.9:c.583G>T	ENSP00000346952.4:p.Asp195Tyr
ENST00000372459.6:c.580G>T	ENSP00000361537.2:p.Asp194Tyr
ENST00000372484.7:c.634G>T	ENSP00000361562.3:p.Asp212Tyr
ENST00000419493.2:c.109G>T	ENSP00000408533.2:p.Asp37Tyr
ENST00000485627.1:n.241G>T
ENST00000606394.5:c.*222G>T	ENSP00000475827.1:n.*222G>T
ENST00000606782.1:n.213G>T
ENST00000606788.5:c.634G>T	ENSP00000476235.1:p.Asp212Tyr
NM_000308.2:c.634G>T	NP_000299.2:p.Asp212Tyr
NM_000308.3:c.634G>T	NP_000299.2:p.Asp212Tyr
NM_001127695.1:c.580G>T	NP_001121167.1:p.Asp194Tyr
NM_001127695.2:c.580G>T	NP_001121167.1:p.Asp194Tyr
NM_001167594.1:c.583G>T	NP_001161066.1:p.Asp195Tyr
NM_001167594.2:c.583G>T	NP_001161066.1:p.Asp195Tyr
NR_133656.1:n.1816G>T
NM_000308.4:c.580G>T MANE Select	NP_000299.3:p.Asp194Tyr
NM_001127695.3:c.580G>T	NP_001121167.1:p.Asp194Tyr
NM_001167594.3:c.529G>T	NP_001161066.2:p.Asp177Tyr
NR_133656.2:n.625G>T