Canonical Allele Identifier: CA409254394

Gene: CTSA

Linked Data

• MyVariant Identifiers: chr20:g.44526721C>G (hg19) ; chr20:g.45898082C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45898082C>G , CM000682.2:g.45898082C>G	GRCh38
NC_000020.10:g.44526721C>G , CM000682.1:g.44526721C>G	GRCh37
NC_000020.9:g.43960128C>G	NCBI36
NG_008291.1:g.12131C>G
NG_012115.1:g.19066G>C
NG_012115.2:g.19066G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000480961.3:n.5469C>G
ENST00000484855.4:n.4087C>G
ENST00000493522.8:n.1699C>G
ENST00000606066.3:n.1823C>G
ENST00000606782.3:n.1453C>G
ENST00000607187.3:n.4256C>G
ENST00000607212.3:n.1543C>G
ENST00000607814.7:n.3083C>G
ENST00000677755.2:n.1752C>G
ENST00000678622.2:n.2623C>G
ENST00000678691.2:n.3580C>G
ENST00000678988.2:n.2710C>G
ENST00000679053.2:n.4454C>G
ENST00000679343.2:n.4793C>G
ENST00000684198.1:n.1947C>G
ENST00000372459.7:c.1332C>G	ENSP00000361537.2:p.Phe444Leu
ENST00000372484.8:c.1386C>G	ENSP00000361562.3:p.Phe462Leu
ENST00000484855.3:n.4087C>G
ENST00000493522.7:n.1699C>G
ENST00000606066.2:n.1471C>G
ENST00000607187.2:n.3770C>G
ENST00000607212.2:n.1543C>G
ENST00000607482.6:c.1332C>G	ENSP00000475524.2:p.Phe444Leu
ENST00000646241.3:c.1332C>G MANE Select	ENSP00000493613.2:p.Phe444Leu
ENST00000676597.1:c.1171C>G	ENSP00000503904.1:n.1171C>G
ENST00000676967.1:c.*725C>G	ENSP00000502866.1:n.*725C>G
ENST00000677394.1:c.1386C>G	ENSP00000504790.1:p.Phe462Leu
ENST00000677525.1:c.*1155C>G	ENSP00000504197.1:n.*1155C>G
ENST00000677755.1:n.1752C>G
ENST00000678025.1:c.*1396C>G	ENSP00000503463.1:n.*1396C>G
ENST00000678078.1:c.*895C>G	ENSP00000502993.1:n.*895C>G
ENST00000678217.1:c.2114C>G	ENSP00000504109.1:n.2114C>G
ENST00000678331.1:c.*50C>G	ENSP00000504524.1:n.*50C>G
ENST00000678443.1:c.1242C>G	ENSP00000504006.1:p.Phe414Leu
ENST00000678512.1:n.5893C>G
ENST00000678622.1:n.2251C>G
ENST00000678691.1:n.3041C>G
ENST00000678939.1:c.*671C>G	ENSP00000503404.1:n.*671C>G
ENST00000678988.1:n.2710C>G
ENST00000679053.1:n.4082C>G
ENST00000679343.1:n.4414C>G
ENST00000191018.9:c.1332C>G	ENSP00000191018.5:p.Phe444Leu
ENST00000354880.9:c.1335C>G	ENSP00000346952.4:p.Phe445Leu
ENST00000372459.6:c.1332C>G	ENSP00000361537.2:p.Phe444Leu
ENST00000372484.7:c.1386C>G	ENSP00000361562.3:p.Phe462Leu
ENST00000484855.2:n.1702C>G
ENST00000606000.1:n.356C>G
ENST00000606788.5:c.*697C>G	ENSP00000476235.1:n.*697C>G
NM_000308.2:c.1386C>G	NP_000299.2:p.Phe462Leu
NM_000308.3:c.1386C>G	NP_000299.2:p.Phe462Leu
NM_001127695.1:c.1332C>G	NP_001121167.1:p.Phe444Leu
NM_001127695.2:c.1332C>G	NP_001121167.1:p.Phe444Leu
NM_001167594.1:c.1335C>G	NP_001161066.1:p.Phe445Leu
NM_001167594.2:c.1335C>G	NP_001161066.1:p.Phe445Leu
NR_133656.1:n.2575C>G
NM_000308.4:c.1332C>G MANE Select	NP_000299.3:p.Phe444Leu
NM_001127695.3:c.1332C>G	NP_001121167.1:p.Phe444Leu
NM_001167594.3:c.1281C>G	NP_001161066.2:p.Phe427Leu
NR_133656.2:n.1384C>G