Canonical Allele Identifier: CA2230664220
Gene: AARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70258065G= , CM000678.2:g.70258065G= GRCh38
NC_000016.9:g.70291968G= , CM000678.1:g.70291968G= GRCh37
NC_000016.8:g.68849469G= NCBI36
NG_023191.1:g.36445C= , LRG_359:g.36445C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261772.13:c.2145C= MANE Select ENSP00000261772.8:p.Gly715=
ENST00000564359.6:n.2150+915C=
ENST00000565361.3:c.2145C= ENSP00000455360.3:p.Gly715=
ENST00000674512.1:c.2124C= ENSP00000501613.1:p.Gly708=
ENST00000674652.1:c.*1934C= ENSP00000502620.1:n.*1934C=
ENST00000674691.1:c.2145C= ENSP00000502247.1:p.Gly715=
ENST00000674768.1:c.*400C= ENSP00000501679.1:n.*400C=
ENST00000674811.1:c.*338C= ENSP00000502055.1:n.*338C=
ENST00000674848.1:n.2194C=
ENST00000674962.1:n.2303C=
ENST00000674963.1:c.2145C= ENSP00000501924.1:p.Gly715=
ENST00000675035.1:c.2145C= ENSP00000502712.1:p.Gly715=
ENST00000675045.1:c.2172C= ENSP00000502014.1:p.Gly724=
ENST00000675120.1:c.*455C= ENSP00000502823.1:n.*455C=
ENST00000675133.1:c.2118C= ENSP00000502230.1:p.Gly706=
ENST00000675270.1:n.2280C=
ENST00000675297.1:c.*497C= ENSP00000502753.1:n.*497C=
ENST00000675371.1:c.1992+915C= ENSP00000502645.1:n.1992+915C=
ENST00000675403.1:n.3065C=
ENST00000675569.1:c.*1379C= ENSP00000502534.1:n.*1379C=
ENST00000675643.1:c.2145C= ENSP00000502797.1:p.Gly715=
ENST00000675691.1:c.2016C= ENSP00000502196.1:p.Gly672=
ENST00000675751.1:c.*1172C= ENSP00000502277.1:n.*1172C=
ENST00000675853.1:c.2145C= ENSP00000502367.1:p.Gly715=
ENST00000675917.1:n.2442C=
ENST00000675953.1:c.2061C= ENSP00000502321.1:p.Gly687=
ENST00000675986.1:n.2303C=
ENST00000676004.1:c.*2144C= ENSP00000502765.1:n.*2144C=
ENST00000676040.1:c.*1379C= ENSP00000502108.1:n.*1379C=
ENST00000676168.1:c.1992+915C= ENSP00000502479.1:n.1992+915C=
ENST00000676209.1:c.*497C= ENSP00000502052.1:n.*497C=
ENST00000676211.1:c.*1172C= ENSP00000502726.1:n.*1172C=
ENST00000676212.1:c.2145C= ENSP00000501853.1:p.Gly715=
ENST00000676247.1:c.*497C= ENSP00000502699.1:n.*497C=
ENST00000261772.12:c.2145C= ENSP00000261772.7:p.Gly715=
ENST00000564359.5:n.488+915C=
ENST00000565361.2:c.490C=
ENST00000569825.1:n.151C=
NM_001605.2:c.2145C= , LRG_359t1:c.2145C= NP_001596.2:p.Gly715=
XR_933220.1:n.2143+915C=
XR_933220.3:n.2102+915C=
NM_001605.3:c.2145C= MANE Select NP_001596.2:p.Gly715=