Canonical Allele Identifier: CA2695229839

Gene: CTSA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45891989_45891990delinsCT , CM000682.2:g.45891989_45891990delinsCT	GRCh38
NC_000020.10:g.44520628_44520629delinsCT , CM000682.1:g.44520628_44520629delinsCT	GRCh37
NC_000020.9:g.43954035_43954036delinsCT	NCBI36
NG_008291.1:g.6038_6039delinsCT
NG_033108.1:g.4298_4299delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480961.3:n.685_686delinsCT
ENST00000484855.4:n.318_319delinsCT
ENST00000493522.8:n.296_297delinsCT
ENST00000606066.3:n.685_686delinsCT
ENST00000606782.3:n.144_145delinsCT
ENST00000607187.3:n.685_686delinsCT
ENST00000607212.3:n.479_480delinsCT
ENST00000607814.7:n.445_446delinsCT
ENST00000677755.2:n.369_370delinsCT
ENST00000678622.2:n.685_686delinsCT
ENST00000678691.2:n.685_686delinsCT
ENST00000678988.2:n.1307_1308delinsCT
ENST00000679053.2:n.685_686delinsCT
ENST00000679343.2:n.685_686delinsCT
ENST00000684198.1:n.685_686delinsCT
ENST00000372459.7:c.268_269delinsCT	ENSP00000361537.2:p.Ser90Leu
ENST00000372484.8:c.322_323delinsCT	ENSP00000361562.3:p.Ser108Leu
ENST00000419493.3:c.268_269delinsCT	ENSP00000408533.3:p.Ser90Leu
ENST00000480961.2:n.295_296delinsCT
ENST00000484855.3:n.318_319delinsCT
ENST00000493522.7:n.296_297delinsCT
ENST00000606066.2:n.333_334delinsCT
ENST00000606394.6:c.248+227_248+228delinsCT	ENSP00000475827.1:n.248+227_248+228delinsCT
ENST00000606782.2:n.144_145delinsCT
ENST00000607187.2:n.199_200delinsCT
ENST00000607212.2:n.479_480delinsCT
ENST00000607482.6:c.268_269delinsCT	ENSP00000475524.2:p.Ser90Leu
ENST00000607814.6:n.445_446delinsCT
ENST00000646241.3:c.268_269delinsCT MANE Select	ENSP00000493613.2:p.Ser90Leu
ENST00000676526.1:c.322_323delinsCT	ENSP00000504209.1:p.Ser108Leu
ENST00000676597.1:c.268_269delinsCT	ENSP00000503904.1:p.Ser90Leu
ENST00000676657.1:c.268_269delinsCT	ENSP00000504158.1:p.Ser90Leu
ENST00000676967.1:c.268_269delinsCT	ENSP00000502866.1:p.Ser90Leu
ENST00000677394.1:c.322_323delinsCT	ENSP00000504790.1:p.Ser108Leu
ENST00000677525.1:c.*91_*92delinsCT	ENSP00000504197.1:n.*91_*92delinsCT
ENST00000677755.1:n.369_370delinsCT
ENST00000678025.1:c.268_269delinsCT	ENSP00000503463.1:p.Ser90Leu
ENST00000678078.1:c.322_323delinsCT	ENSP00000502993.1:p.Ser108Leu
ENST00000678217.1:c.268_269delinsCT	ENSP00000504109.1:p.Ser90Leu
ENST00000678331.1:c.268_269delinsCT	ENSP00000504524.1:p.Ser90Leu
ENST00000678443.1:c.268_269delinsCT	ENSP00000504006.1:p.Ser90Leu
ENST00000678512.1:n.458_459delinsCT
ENST00000678622.1:n.313_314delinsCT
ENST00000678691.1:n.146_147delinsCT
ENST00000678939.1:c.268_269delinsCT	ENSP00000503404.1:p.Ser90Leu
ENST00000678988.1:n.1307_1308delinsCT
ENST00000679053.1:n.313_314delinsCT
ENST00000679343.1:n.306_307delinsCT
ENST00000191018.9:c.268_269delinsCT	ENSP00000191018.5:p.Ser90Leu
ENST00000354880.9:c.322_323delinsCT	ENSP00000346952.4:p.Ser108Leu
ENST00000372459.6:c.268_269delinsCT	ENSP00000361537.2:p.Ser90Leu
ENST00000372484.7:c.322_323delinsCT	ENSP00000361562.3:p.Ser108Leu
ENST00000606066.1:n.313_314delinsCT
ENST00000606394.5:c.248+227_248+228delinsCT	ENSP00000475827.1:n.248+227_248+228delinsCT
ENST00000606788.5:c.322_323delinsCT	ENSP00000476235.1:p.Ser108Leu
ENST00000607212.1:n.444_445delinsCT
ENST00000607482.5:c.268_269delinsCT	ENSP00000475524.1:p.Ser90Leu
ENST00000607814.5:n.446_447delinsCT
ENST00000607841.5:n.313_314delinsCT
NM_000308.2:c.322_323delinsCT	NP_000299.2:p.Ser108Leu
NM_000308.3:c.322_323delinsCT	NP_000299.2:p.Ser108Leu
NM_001127695.1:c.268_269delinsCT	NP_001121167.1:p.Ser90Leu
NM_001127695.2:c.268_269delinsCT	NP_001121167.1:p.Ser90Leu
NM_001167594.1:c.322_323delinsCT	NP_001161066.1:p.Ser108Leu
NM_001167594.2:c.322_323delinsCT	NP_001161066.1:p.Ser108Leu
NR_133656.1:n.1504_1505delinsCT
NM_000308.4:c.268_269delinsCT MANE Select	NP_000299.3:p.Ser90Leu
NM_001127695.3:c.268_269delinsCT	NP_001121167.1:p.Ser90Leu
NM_001167594.3:c.268_269delinsCT	NP_001161066.2:p.Ser90Leu
NR_133656.2:n.313_314delinsCT