Canonical Allele Identifier: CA396557529

Gene: AARS1

Linked Data

• MyVariant Identifiers: chr16:g.70291948A>T (hg19) ; chr16:g.70258045A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70258045A>T , CM000678.2:g.70258045A>T	GRCh38
NC_000016.9:g.70291948A>T , CM000678.1:g.70291948A>T	GRCh37
NC_000016.8:g.68849449A>T	NCBI36
NG_023191.1:g.36465T>A , LRG_359:g.36465T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261772.13:c.2165T>A MANE Select	ENSP00000261772.8:p.Phe722Tyr
ENST00000564359.6:n.2150+935T>A
ENST00000565361.3:c.2165T>A	ENSP00000455360.3:p.Phe722Tyr
ENST00000674512.1:c.2144T>A	ENSP00000501613.1:p.Phe715Tyr
ENST00000674652.1:c.*1954T>A	ENSP00000502620.1:n.*1954T>A
ENST00000674691.1:c.2165T>A	ENSP00000502247.1:p.Phe722Tyr
ENST00000674768.1:c.*420T>A	ENSP00000501679.1:n.*420T>A
ENST00000674811.1:c.*358T>A	ENSP00000502055.1:n.*358T>A
ENST00000674848.1:n.2214T>A
ENST00000674962.1:n.2323T>A
ENST00000674963.1:c.2165T>A	ENSP00000501924.1:p.Phe722Tyr
ENST00000675035.1:c.2157+8T>A	ENSP00000502712.1:n.2157+8T>A
ENST00000675045.1:c.2192T>A	ENSP00000502014.1:p.Phe731Tyr
ENST00000675120.1:c.*475T>A	ENSP00000502823.1:n.*475T>A
ENST00000675133.1:c.2138T>A	ENSP00000502230.1:p.Phe713Tyr
ENST00000675270.1:n.2300T>A
ENST00000675297.1:c.*517T>A	ENSP00000502753.1:n.*517T>A
ENST00000675371.1:c.1992+935T>A	ENSP00000502645.1:n.1992+935T>A
ENST00000675403.1:n.3085T>A
ENST00000675569.1:c.*1399T>A	ENSP00000502534.1:n.*1399T>A
ENST00000675643.1:c.2165T>A	ENSP00000502797.1:p.Phe722Tyr
ENST00000675691.1:c.2036T>A	ENSP00000502196.1:p.Phe679Tyr
ENST00000675751.1:c.*1192T>A	ENSP00000502277.1:n.*1192T>A
ENST00000675853.1:c.2165T>A	ENSP00000502367.1:p.Phe722Tyr
ENST00000675917.1:n.2462T>A
ENST00000675953.1:c.2081T>A	ENSP00000502321.1:p.Phe694Tyr
ENST00000675986.1:n.2323T>A
ENST00000676004.1:c.*2164T>A	ENSP00000502765.1:n.*2164T>A
ENST00000676040.1:c.*1399T>A	ENSP00000502108.1:n.*1399T>A
ENST00000676168.1:c.1992+935T>A	ENSP00000502479.1:n.1992+935T>A
ENST00000676209.1:c.*517T>A	ENSP00000502052.1:n.*517T>A
ENST00000676211.1:c.*1192T>A	ENSP00000502726.1:n.*1192T>A
ENST00000676212.1:c.2165T>A	ENSP00000501853.1:p.Phe722Tyr
ENST00000676247.1:c.*517T>A	ENSP00000502699.1:n.*517T>A
ENST00000261772.12:c.2165T>A	ENSP00000261772.7:p.Phe722Tyr
ENST00000564359.5:n.488+935T>A
ENST00000565361.2:c.510T>A
ENST00000569825.1:n.171T>A
NM_001605.2:c.2165T>A , LRG_359t1:c.2165T>A	NP_001596.2:p.Phe722Tyr
XR_933220.1:n.2143+935T>A
XR_933220.3:n.2102+935T>A
NM_001605.3:c.2165T>A MANE Select	NP_001596.2:p.Phe722Tyr