Canonical Allele Identifier: CA510638299

Gene: CTSA

Linked Data

• MyVariant Identifiers: chr20:g.44521501T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.45892862T>C , CM000682.2:g.45892862T>C	GRCh38
NC_000020.10:g.44521501T>C , CM000682.1:g.44521501T>C	GRCh37
NC_000020.9:g.43954908T>C	NCBI36
NG_008291.1:g.6911T>C
NG_033108.1:g.3426A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480961.3:n.999T>C
ENST00000484855.4:n.632T>C
ENST00000493522.8:n.610T>C
ENST00000606066.3:n.1073T>C
ENST00000606782.3:n.703T>C
ENST00000607187.3:n.999T>C
ENST00000607212.3:n.793T>C
ENST00000607814.7:n.1318T>C
ENST00000677755.2:n.1002T>C
ENST00000678622.2:n.999T>C
ENST00000678691.2:n.999T>C
ENST00000678988.2:n.1621T>C
ENST00000679053.2:n.999T>C
ENST00000679343.2:n.999T>C
ENST00000684198.1:n.999T>C
ENST00000372459.7:c.582T>C	ENSP00000361537.2:p.Asp194=
ENST00000372484.8:c.636T>C	ENSP00000361562.3:p.Asp212=
ENST00000419493.3:c.582T>C	ENSP00000408533.3:p.Asp194=
ENST00000480961.2:n.609T>C
ENST00000484855.3:n.632T>C
ENST00000493522.7:n.610T>C
ENST00000606066.2:n.721T>C
ENST00000606394.6:c.*224T>C	ENSP00000475827.1:n.*224T>C
ENST00000606782.2:n.703T>C
ENST00000607187.2:n.513T>C
ENST00000607212.2:n.793T>C
ENST00000607482.6:c.582T>C	ENSP00000475524.2:p.Asp194=
ENST00000607814.6:n.1318T>C
ENST00000646241.3:c.582T>C MANE Select	ENSP00000493613.2:p.Asp194=
ENST00000676526.1:c.636T>C	ENSP00000504209.1:p.Asp212=
ENST00000676597.1:c.582T>C	ENSP00000503904.1:p.Asp194=
ENST00000676657.1:c.582T>C	ENSP00000504158.1:p.Asp194=
ENST00000676967.1:c.582T>C	ENSP00000502866.1:p.Asp194=
ENST00000677394.1:c.636T>C	ENSP00000504790.1:p.Asp212=
ENST00000677525.1:c.*405T>C	ENSP00000504197.1:n.*405T>C
ENST00000677755.1:n.1002T>C
ENST00000678025.1:c.582T>C	ENSP00000503463.1:p.Asp194=
ENST00000678078.1:c.636T>C	ENSP00000502993.1:p.Asp212=
ENST00000678217.1:c.582T>C	ENSP00000504109.1:p.Asp194=
ENST00000678331.1:c.582T>C	ENSP00000504524.1:p.Asp194=
ENST00000678443.1:c.582T>C	ENSP00000504006.1:p.Asp194=
ENST00000678512.1:n.846T>C
ENST00000678622.1:n.627T>C
ENST00000678691.1:n.460T>C
ENST00000678939.1:c.582T>C	ENSP00000503404.1:p.Asp194=
ENST00000678988.1:n.1621T>C
ENST00000679053.1:n.627T>C
ENST00000679343.1:n.620T>C
ENST00000191018.9:c.582T>C	ENSP00000191018.5:p.Asp194=
ENST00000354880.9:c.585T>C	ENSP00000346952.4:p.Asp195=
ENST00000372459.6:c.582T>C	ENSP00000361537.2:p.Asp194=
ENST00000372484.7:c.636T>C	ENSP00000361562.3:p.Asp212=
ENST00000419493.2:c.111T>C	ENSP00000408533.2:p.Asp37=
ENST00000485627.1:n.243T>C
ENST00000606394.5:c.*224T>C	ENSP00000475827.1:n.*224T>C
ENST00000606782.1:n.215T>C
ENST00000606788.5:c.636T>C	ENSP00000476235.1:p.Asp212=
NM_000308.2:c.636T>C	NP_000299.2:p.Asp212=
NM_000308.3:c.636T>C	NP_000299.2:p.Asp212=
NM_001127695.1:c.582T>C	NP_001121167.1:p.Asp194=
NM_001127695.2:c.582T>C	NP_001121167.1:p.Asp194=
NM_001167594.1:c.585T>C	NP_001161066.1:p.Asp195=
NM_001167594.2:c.585T>C	NP_001161066.1:p.Asp195=
NR_133656.1:n.1818T>C
NM_000308.4:c.582T>C MANE Select	NP_000299.3:p.Asp194=
NM_001127695.3:c.582T>C	NP_001121167.1:p.Asp194=
NM_001167594.3:c.531T>C	NP_001161066.2:p.Asp177=
NR_133656.2:n.627T>C