Canonical Allele Identifier: CA396557538

Gene: AARS1

Linked Data

• ClinVar Variation Id: 2038644
• ClinVar RCV Id: RCV002895111
• MyVariant Identifiers: chr16:g.70291951T>G (hg19) ; chr16:g.70258048T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70258048T>G , CM000678.2:g.70258048T>G	GRCh38
NC_000016.9:g.70291951T>G , CM000678.1:g.70291951T>G	GRCh37
NC_000016.8:g.68849452T>G	NCBI36
NG_023191.1:g.36462A>C , LRG_359:g.36462A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261772.13:c.2162A>C MANE Select	ENSP00000261772.8:p.Glu721Ala
ENST00000564359.6:n.2150+932A>C
ENST00000565361.3:c.2162A>C	ENSP00000455360.3:p.Glu721Ala
ENST00000674512.1:c.2141A>C	ENSP00000501613.1:p.Glu714Ala
ENST00000674652.1:c.*1951A>C	ENSP00000502620.1:n.*1951A>C
ENST00000674691.1:c.2162A>C	ENSP00000502247.1:p.Glu721Ala
ENST00000674768.1:c.*417A>C	ENSP00000501679.1:n.*417A>C
ENST00000674811.1:c.*355A>C	ENSP00000502055.1:n.*355A>C
ENST00000674848.1:n.2211A>C
ENST00000674962.1:n.2320A>C
ENST00000674963.1:c.2162A>C	ENSP00000501924.1:p.Glu721Ala
ENST00000675035.1:c.2157+5A>C	ENSP00000502712.1:n.2157+5A>C
ENST00000675045.1:c.2189A>C	ENSP00000502014.1:p.Glu730Ala
ENST00000675120.1:c.*472A>C	ENSP00000502823.1:n.*472A>C
ENST00000675133.1:c.2135A>C	ENSP00000502230.1:p.Glu712Ala
ENST00000675270.1:n.2297A>C
ENST00000675297.1:c.*514A>C	ENSP00000502753.1:n.*514A>C
ENST00000675371.1:c.1992+932A>C	ENSP00000502645.1:n.1992+932A>C
ENST00000675403.1:n.3082A>C
ENST00000675569.1:c.*1396A>C	ENSP00000502534.1:n.*1396A>C
ENST00000675643.1:c.2162A>C	ENSP00000502797.1:p.Glu721Ala
ENST00000675691.1:c.2033A>C	ENSP00000502196.1:p.Glu678Ala
ENST00000675751.1:c.*1189A>C	ENSP00000502277.1:n.*1189A>C
ENST00000675853.1:c.2162A>C	ENSP00000502367.1:p.Glu721Ala
ENST00000675917.1:n.2459A>C
ENST00000675953.1:c.2078A>C	ENSP00000502321.1:p.Glu693Ala
ENST00000675986.1:n.2320A>C
ENST00000676004.1:c.*2161A>C	ENSP00000502765.1:n.*2161A>C
ENST00000676040.1:c.*1396A>C	ENSP00000502108.1:n.*1396A>C
ENST00000676168.1:c.1992+932A>C	ENSP00000502479.1:n.1992+932A>C
ENST00000676209.1:c.*514A>C	ENSP00000502052.1:n.*514A>C
ENST00000676211.1:c.*1189A>C	ENSP00000502726.1:n.*1189A>C
ENST00000676212.1:c.2162A>C	ENSP00000501853.1:p.Glu721Ala
ENST00000676247.1:c.*514A>C	ENSP00000502699.1:n.*514A>C
ENST00000261772.12:c.2162A>C	ENSP00000261772.7:p.Glu721Ala
ENST00000564359.5:n.488+932A>C
ENST00000565361.2:c.507A>C
ENST00000569825.1:n.168A>C
NM_001605.2:c.2162A>C , LRG_359t1:c.2162A>C	NP_001596.2:p.Glu721Ala
XR_933220.1:n.2143+932A>C
XR_933220.3:n.2102+932A>C
NM_001605.3:c.2162A>C MANE Select	NP_001596.2:p.Glu721Ala