Canonical Allele Identifier: CA2230664318
Gene: AARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70258101C= , CM000678.2:g.70258101C= GRCh38
NC_000016.9:g.70292004C= , CM000678.1:g.70292004C= GRCh37
NC_000016.8:g.68849505C= NCBI36
NG_023191.1:g.36409G= , LRG_359:g.36409G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261772.13:c.2109G= MANE Select ENSP00000261772.8:p.Val703=
ENST00000564359.6:n.2150+879G=
ENST00000565361.3:c.2109G= ENSP00000455360.3:p.Val703=
ENST00000674512.1:c.2088G= ENSP00000501613.1:p.Val696=
ENST00000674652.1:c.*1898G= ENSP00000502620.1:n.*1898G=
ENST00000674691.1:c.2109G= ENSP00000502247.1:p.Val703=
ENST00000674768.1:c.*364G= ENSP00000501679.1:n.*364G=
ENST00000674811.1:c.*302G= ENSP00000502055.1:n.*302G=
ENST00000674848.1:n.2158G=
ENST00000674962.1:n.2267G=
ENST00000674963.1:c.2109G= ENSP00000501924.1:p.Val703=
ENST00000675035.1:c.2109G= ENSP00000502712.1:p.Val703=
ENST00000675045.1:c.2136G= ENSP00000502014.1:p.Val712=
ENST00000675120.1:c.*419G= ENSP00000502823.1:n.*419G=
ENST00000675133.1:c.2082G= ENSP00000502230.1:p.Val694=
ENST00000675270.1:n.2244G=
ENST00000675297.1:c.*461G= ENSP00000502753.1:n.*461G=
ENST00000675371.1:c.1992+879G= ENSP00000502645.1:n.1992+879G=
ENST00000675403.1:n.3029G=
ENST00000675569.1:c.*1343G= ENSP00000502534.1:n.*1343G=
ENST00000675643.1:c.2109G= ENSP00000502797.1:p.Val703=
ENST00000675691.1:c.1980G= ENSP00000502196.1:p.Val660=
ENST00000675751.1:c.*1136G= ENSP00000502277.1:n.*1136G=
ENST00000675853.1:c.2109G= ENSP00000502367.1:p.Val703=
ENST00000675917.1:n.2406G=
ENST00000675953.1:c.2025G= ENSP00000502321.1:p.Val675=
ENST00000675986.1:n.2267G=
ENST00000676004.1:c.*2108G= ENSP00000502765.1:n.*2108G=
ENST00000676040.1:c.*1343G= ENSP00000502108.1:n.*1343G=
ENST00000676168.1:c.1992+879G= ENSP00000502479.1:n.1992+879G=
ENST00000676209.1:c.*461G= ENSP00000502052.1:n.*461G=
ENST00000676211.1:c.*1136G= ENSP00000502726.1:n.*1136G=
ENST00000676212.1:c.2109G= ENSP00000501853.1:p.Val703=
ENST00000676247.1:c.*461G= ENSP00000502699.1:n.*461G=
ENST00000261772.12:c.2109G= ENSP00000261772.7:p.Val703=
ENST00000564359.5:n.488+879G=
ENST00000565361.2:c.454G=
ENST00000569825.1:n.115G=
NM_001605.2:c.2109G= , LRG_359t1:c.2109G= NP_001596.2:p.Val703=
XR_933220.1:n.2143+879G=
XR_933220.3:n.2102+879G=
NM_001605.3:c.2109G= MANE Select NP_001596.2:p.Val703=