Canonical Allele Identifier: CA2230664413
Gene: AARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70258131A= , CM000678.2:g.70258131A= GRCh38
NC_000016.9:g.70292034A= , CM000678.1:g.70292034A= GRCh37
NC_000016.8:g.68849535A= NCBI36
NG_023191.1:g.36379T= , LRG_359:g.36379T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261772.13:c.2079T= MANE Select ENSP00000261772.8:p.Pro693=
ENST00000564359.6:n.2150+849T=
ENST00000565361.3:c.2079T= ENSP00000455360.3:p.Pro693=
ENST00000674512.1:c.2058T= ENSP00000501613.1:p.Pro686=
ENST00000674652.1:c.*1868T= ENSP00000502620.1:n.*1868T=
ENST00000674691.1:c.2079T= ENSP00000502247.1:p.Pro693=
ENST00000674768.1:c.*334T= ENSP00000501679.1:n.*334T=
ENST00000674811.1:c.*272T= ENSP00000502055.1:n.*272T=
ENST00000674848.1:n.2128T=
ENST00000674962.1:n.2237T=
ENST00000674963.1:c.2079T= ENSP00000501924.1:p.Pro693=
ENST00000675035.1:c.2079T= ENSP00000502712.1:p.Pro693=
ENST00000675045.1:c.2106T= ENSP00000502014.1:p.Pro702=
ENST00000675120.1:c.*389T= ENSP00000502823.1:n.*389T=
ENST00000675133.1:c.2052T= ENSP00000502230.1:p.Pro684=
ENST00000675270.1:n.2214T=
ENST00000675297.1:c.*431T= ENSP00000502753.1:n.*431T=
ENST00000675371.1:c.1992+849T= ENSP00000502645.1:n.1992+849T=
ENST00000675403.1:n.2999T=
ENST00000675569.1:c.*1313T= ENSP00000502534.1:n.*1313T=
ENST00000675643.1:c.2079T= ENSP00000502797.1:p.Pro693=
ENST00000675691.1:c.1950T= ENSP00000502196.1:p.Pro650=
ENST00000675751.1:c.*1106T= ENSP00000502277.1:n.*1106T=
ENST00000675853.1:c.2079T= ENSP00000502367.1:p.Pro693=
ENST00000675917.1:n.2376T=
ENST00000675953.1:c.1995T= ENSP00000502321.1:p.Pro665=
ENST00000675986.1:n.2237T=
ENST00000676004.1:c.*2078T= ENSP00000502765.1:n.*2078T=
ENST00000676040.1:c.*1313T= ENSP00000502108.1:n.*1313T=
ENST00000676168.1:c.1992+849T= ENSP00000502479.1:n.1992+849T=
ENST00000676209.1:c.*431T= ENSP00000502052.1:n.*431T=
ENST00000676211.1:c.*1106T= ENSP00000502726.1:n.*1106T=
ENST00000676212.1:c.2079T= ENSP00000501853.1:p.Pro693=
ENST00000676247.1:c.*431T= ENSP00000502699.1:n.*431T=
ENST00000261772.12:c.2079T= ENSP00000261772.7:p.Pro693=
ENST00000564359.5:n.488+849T=
ENST00000565361.2:c.424T=
ENST00000569825.1:n.85T=
NM_001605.2:c.2079T= , LRG_359t1:c.2079T= NP_001596.2:p.Pro693=
XR_933220.1:n.2143+849T=
XR_933220.3:n.2102+849T=
NM_001605.3:c.2079T= MANE Select NP_001596.2:p.Pro693=