Canonical Allele Identifier: CA409254371

Gene: CTSA

Linked Data

• MyVariant Identifiers: chr20:g.44526713A>C (hg19) ; chr20:g.45898074A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45898074A>C , CM000682.2:g.45898074A>C	GRCh38
NC_000020.10:g.44526713A>C , CM000682.1:g.44526713A>C	GRCh37
NC_000020.9:g.43960120A>C	NCBI36
NG_008291.1:g.12123A>C
NG_012115.1:g.19074T>G
NG_012115.2:g.19074T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000480961.3:n.5461A>C
ENST00000484855.4:n.4079A>C
ENST00000493522.8:n.1691A>C
ENST00000606066.3:n.1815A>C
ENST00000606782.3:n.1445A>C
ENST00000607187.3:n.4248A>C
ENST00000607212.3:n.1535A>C
ENST00000607814.7:n.3075A>C
ENST00000677755.2:n.1744A>C
ENST00000678622.2:n.2615A>C
ENST00000678691.2:n.3572A>C
ENST00000678988.2:n.2702A>C
ENST00000679053.2:n.4446A>C
ENST00000679343.2:n.4785A>C
ENST00000684198.1:n.1939A>C
ENST00000372459.7:c.1324A>C	ENSP00000361537.2:p.Lys442Gln
ENST00000372484.8:c.1378A>C	ENSP00000361562.3:p.Lys460Gln
ENST00000484855.3:n.4079A>C
ENST00000493522.7:n.1691A>C
ENST00000606066.2:n.1463A>C
ENST00000607187.2:n.3762A>C
ENST00000607212.2:n.1535A>C
ENST00000607482.6:c.1324A>C	ENSP00000475524.2:p.Lys442Gln
ENST00000646241.3:c.1324A>C MANE Select	ENSP00000493613.2:p.Lys442Gln
ENST00000676597.1:c.1163A>C	ENSP00000503904.1:n.1163A>C
ENST00000676967.1:c.*717A>C	ENSP00000502866.1:n.*717A>C
ENST00000677394.1:c.1378A>C	ENSP00000504790.1:p.Lys460Gln
ENST00000677525.1:c.*1147A>C	ENSP00000504197.1:n.*1147A>C
ENST00000677755.1:n.1744A>C
ENST00000678025.1:c.*1388A>C	ENSP00000503463.1:n.*1388A>C
ENST00000678078.1:c.*887A>C	ENSP00000502993.1:n.*887A>C
ENST00000678217.1:c.2106A>C	ENSP00000504109.1:n.2106A>C
ENST00000678331.1:c.*42A>C	ENSP00000504524.1:n.*42A>C
ENST00000678443.1:c.1234A>C	ENSP00000504006.1:p.Lys412Gln
ENST00000678512.1:n.5885A>C
ENST00000678622.1:n.2243A>C
ENST00000678691.1:n.3033A>C
ENST00000678939.1:c.*663A>C	ENSP00000503404.1:n.*663A>C
ENST00000678988.1:n.2702A>C
ENST00000679053.1:n.4074A>C
ENST00000679343.1:n.4406A>C
ENST00000191018.9:c.1324A>C	ENSP00000191018.5:p.Lys442Gln
ENST00000354880.9:c.1327A>C	ENSP00000346952.4:p.Lys443Gln
ENST00000372459.6:c.1324A>C	ENSP00000361537.2:p.Lys442Gln
ENST00000372484.7:c.1378A>C	ENSP00000361562.3:p.Lys460Gln
ENST00000484855.2:n.1694A>C
ENST00000606000.1:n.348A>C
ENST00000606788.5:c.*689A>C	ENSP00000476235.1:n.*689A>C
NM_000308.2:c.1378A>C	NP_000299.2:p.Lys460Gln
NM_000308.3:c.1378A>C	NP_000299.2:p.Lys460Gln
NM_001127695.1:c.1324A>C	NP_001121167.1:p.Lys442Gln
NM_001127695.2:c.1324A>C	NP_001121167.1:p.Lys442Gln
NM_001167594.1:c.1327A>C	NP_001161066.1:p.Lys443Gln
NM_001167594.2:c.1327A>C	NP_001161066.1:p.Lys443Gln
NR_133656.1:n.2567A>C
NM_000308.4:c.1324A>C MANE Select	NP_000299.3:p.Lys442Gln
NM_001127695.3:c.1324A>C	NP_001121167.1:p.Lys442Gln
NM_001167594.3:c.1273A>C	NP_001161066.2:p.Lys425Gln
NR_133656.2:n.1376A>C