Canonical Allele Identifier: CA2230664208
Gene: AARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70258057G= , CM000678.2:g.70258057G= GRCh38
NC_000016.9:g.70291960G= , CM000678.1:g.70291960G= GRCh37
NC_000016.8:g.68849461G= NCBI36
NG_023191.1:g.36453C= , LRG_359:g.36453C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261772.13:c.2153C= MANE Select ENSP00000261772.8:p.Thr718=
ENST00000564359.6:n.2150+923C=
ENST00000565361.3:c.2153C= ENSP00000455360.3:p.Thr718=
ENST00000674512.1:c.2132C= ENSP00000501613.1:p.Thr711=
ENST00000674652.1:c.*1942C= ENSP00000502620.1:n.*1942C=
ENST00000674691.1:c.2153C= ENSP00000502247.1:p.Thr718=
ENST00000674768.1:c.*408C= ENSP00000501679.1:n.*408C=
ENST00000674811.1:c.*346C= ENSP00000502055.1:n.*346C=
ENST00000674848.1:n.2202C=
ENST00000674962.1:n.2311C=
ENST00000674963.1:c.2153C= ENSP00000501924.1:p.Thr718=
ENST00000675035.1:c.2153C= ENSP00000502712.1:p.Thr718=
ENST00000675045.1:c.2180C= ENSP00000502014.1:p.Thr727=
ENST00000675120.1:c.*463C= ENSP00000502823.1:n.*463C=
ENST00000675133.1:c.2126C= ENSP00000502230.1:p.Thr709=
ENST00000675270.1:n.2288C=
ENST00000675297.1:c.*505C= ENSP00000502753.1:n.*505C=
ENST00000675371.1:c.1992+923C= ENSP00000502645.1:n.1992+923C=
ENST00000675403.1:n.3073C=
ENST00000675569.1:c.*1387C= ENSP00000502534.1:n.*1387C=
ENST00000675643.1:c.2153C= ENSP00000502797.1:p.Thr718=
ENST00000675691.1:c.2024C= ENSP00000502196.1:p.Thr675=
ENST00000675751.1:c.*1180C= ENSP00000502277.1:n.*1180C=
ENST00000675853.1:c.2153C= ENSP00000502367.1:p.Thr718=
ENST00000675917.1:n.2450C=
ENST00000675953.1:c.2069C= ENSP00000502321.1:p.Thr690=
ENST00000675986.1:n.2311C=
ENST00000676004.1:c.*2152C= ENSP00000502765.1:n.*2152C=
ENST00000676040.1:c.*1387C= ENSP00000502108.1:n.*1387C=
ENST00000676168.1:c.1992+923C= ENSP00000502479.1:n.1992+923C=
ENST00000676209.1:c.*505C= ENSP00000502052.1:n.*505C=
ENST00000676211.1:c.*1180C= ENSP00000502726.1:n.*1180C=
ENST00000676212.1:c.2153C= ENSP00000501853.1:p.Thr718=
ENST00000676247.1:c.*505C= ENSP00000502699.1:n.*505C=
ENST00000261772.12:c.2153C= ENSP00000261772.7:p.Thr718=
ENST00000564359.5:n.488+923C=
ENST00000565361.2:c.498C=
ENST00000569825.1:n.159C=
NM_001605.2:c.2153C= , LRG_359t1:c.2153C= NP_001596.2:p.Thr718=
XR_933220.1:n.2143+923C=
XR_933220.3:n.2102+923C=
NM_001605.3:c.2153C= MANE Select NP_001596.2:p.Thr718=