Canonical Allele Identifier: CA2230664476
Gene: AARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70258161C= , CM000678.2:g.70258161C= GRCh38
NC_000016.9:g.70292064C= , CM000678.1:g.70292064C= GRCh37
NC_000016.8:g.68849565C= NCBI36
NG_023191.1:g.36349G= , LRG_359:g.36349G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261772.13:c.2049G= MANE Select ENSP00000261772.8:p.Arg683=
ENST00000564359.6:n.2150+819G=
ENST00000565361.3:c.2049G= ENSP00000455360.3:p.Arg683=
ENST00000674512.1:c.2028G= ENSP00000501613.1:p.Arg676=
ENST00000674652.1:c.*1838G= ENSP00000502620.1:n.*1838G=
ENST00000674691.1:c.2049G= ENSP00000502247.1:p.Arg683=
ENST00000674768.1:c.*304G= ENSP00000501679.1:n.*304G=
ENST00000674811.1:c.*242G= ENSP00000502055.1:n.*242G=
ENST00000674848.1:n.2098G=
ENST00000674962.1:n.2207G=
ENST00000674963.1:c.2049G= ENSP00000501924.1:p.Arg683=
ENST00000675035.1:c.2049G= ENSP00000502712.1:p.Arg683=
ENST00000675045.1:c.2076G= ENSP00000502014.1:p.Arg692=
ENST00000675120.1:c.*359G= ENSP00000502823.1:n.*359G=
ENST00000675133.1:c.2022G= ENSP00000502230.1:p.Arg674=
ENST00000675270.1:n.2184G=
ENST00000675297.1:c.*401G= ENSP00000502753.1:n.*401G=
ENST00000675371.1:c.1992+819G= ENSP00000502645.1:n.1992+819G=
ENST00000675403.1:n.2969G=
ENST00000675569.1:c.*1283G= ENSP00000502534.1:n.*1283G=
ENST00000675643.1:c.2049G= ENSP00000502797.1:p.Arg683=
ENST00000675691.1:c.1920G= ENSP00000502196.1:p.Arg640=
ENST00000675751.1:c.*1076G= ENSP00000502277.1:n.*1076G=
ENST00000675853.1:c.2049G= ENSP00000502367.1:p.Arg683=
ENST00000675917.1:n.2346G=
ENST00000675953.1:c.1965G= ENSP00000502321.1:p.Arg655=
ENST00000675986.1:n.2207G=
ENST00000676004.1:c.*2048G= ENSP00000502765.1:n.*2048G=
ENST00000676040.1:c.*1283G= ENSP00000502108.1:n.*1283G=
ENST00000676168.1:c.1992+819G= ENSP00000502479.1:n.1992+819G=
ENST00000676209.1:c.*401G= ENSP00000502052.1:n.*401G=
ENST00000676211.1:c.*1076G= ENSP00000502726.1:n.*1076G=
ENST00000676212.1:c.2049G= ENSP00000501853.1:p.Arg683=
ENST00000676247.1:c.*401G= ENSP00000502699.1:n.*401G=
ENST00000261772.12:c.2049G= ENSP00000261772.7:p.Arg683=
ENST00000564359.5:n.488+819G=
ENST00000565361.2:c.394G=
ENST00000569825.1:n.55G=
NM_001605.2:c.2049G= , LRG_359t1:c.2049G= NP_001596.2:p.Arg683=
XR_933220.1:n.2143+819G=
XR_933220.3:n.2102+819G=
NM_001605.3:c.2049G= MANE Select NP_001596.2:p.Arg683=