Canonical Allele Identifier: CA8140651

Gene: AARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70259148C>T , CM000678.2:g.70259148C>T	GRCh38
NC_000016.9:g.70293051C>T , CM000678.1:g.70293051C>T	GRCh37
NC_000016.8:g.68850552C>T	NCBI36
NG_023191.1:g.35362G>A , LRG_359:g.35362G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001605.3:c.1824G>A MANE Select	NP_001596.2:p.Thr608=
ENST00000261772.13:c.1824G>A MANE Select	ENSP00000261772.8:p.Thr608=
NM_001605.2:c.1824G>A , LRG_359t1:c.1824G>A	NP_001596.2:p.Thr608=
ENST00000261772.12:c.1824G>A	ENSP00000261772.7:p.Thr608=
ENST00000564359.5:n.320G>A
ENST00000564359.6:n.1982G>A
ENST00000565361.2:c.169G>A
ENST00000565361.3:c.1824G>A	ENSP00000455360.3:p.Thr608=
ENST00000567490.1:n.409G>A
ENST00000569790.2:n.416G>A
ENST00000674512.1:c.1803G>A	ENSP00000501613.1:p.Thr601=
ENST00000674652.1:c.*851G>A	ENSP00000502620.1:n.*851G>A
ENST00000674691.1:c.1824G>A	ENSP00000502247.1:p.Thr608=
ENST00000674768.1:c.*79G>A	ENSP00000501679.1:n.*79G>A
ENST00000674811.1:c.*17G>A	ENSP00000502055.1:n.*17G>A
ENST00000674848.1:n.1873G>A
ENST00000674962.1:n.1982G>A
ENST00000674963.1:c.1824G>A	ENSP00000501924.1:p.Thr608=
ENST00000675035.1:c.1824G>A	ENSP00000502712.1:p.Thr608=
ENST00000675045.1:c.1824G>A	ENSP00000502014.1:p.Thr608=
ENST00000675120.1:c.*134G>A	ENSP00000502823.1:n.*134G>A
ENST00000675133.1:c.1797G>A	ENSP00000502230.1:p.Thr599=
ENST00000675270.1:n.1959G>A
ENST00000675297.1:c.*176G>A	ENSP00000502753.1:n.*176G>A
ENST00000675371.1:c.1824G>A	ENSP00000502645.1:p.Thr608=
ENST00000675403.1:n.1982G>A
ENST00000675569.1:c.*1058G>A	ENSP00000502534.1:n.*1058G>A
ENST00000675643.1:c.1824G>A	ENSP00000502797.1:p.Thr608=
ENST00000675691.1:c.1695G>A	ENSP00000502196.1:p.Thr565=
ENST00000675751.1:c.*851G>A	ENSP00000502277.1:n.*851G>A
ENST00000675853.1:c.1824G>A	ENSP00000502367.1:p.Thr608=
ENST00000675917.1:n.2121G>A
ENST00000675953.1:c.1740G>A	ENSP00000502321.1:p.Thr580=
ENST00000675986.1:n.1982G>A
ENST00000676004.1:c.*1823G>A	ENSP00000502765.1:n.*1823G>A
ENST00000676040.1:c.*1058G>A	ENSP00000502108.1:n.*1058G>A
ENST00000676168.1:c.1824G>A	ENSP00000502479.1:p.Thr608=
ENST00000676209.1:c.*176G>A	ENSP00000502052.1:n.*176G>A
ENST00000676211.1:c.*851G>A	ENSP00000502726.1:n.*851G>A
ENST00000676212.1:c.1824G>A	ENSP00000501853.1:p.Thr608=
ENST00000676247.1:c.*176G>A	ENSP00000502699.1:n.*176G>A
XR_933220.1:n.1975G>A
XR_933220.3:n.1934G>A