Canonical Allele Identifier: CA396557773

Gene: AARS1

Linked Data

• gnomAD v4: 16-70258170-C-A
• MyVariant Identifiers: chr16:g.70292073C>A (hg19) ; chr16:g.70258170C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70258170C>A , CM000678.2:g.70258170C>A	GRCh38
NC_000016.9:g.70292073C>A , CM000678.1:g.70292073C>A	GRCh37
NC_000016.8:g.68849574C>A	NCBI36
NG_023191.1:g.36340G>T , LRG_359:g.36340G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261772.13:c.2040G>T MANE Select	ENSP00000261772.8:p.Gln680His
ENST00000564359.6:n.2150+810G>T
ENST00000565361.3:c.2040G>T	ENSP00000455360.3:p.Gln680His
ENST00000674512.1:c.2019G>T	ENSP00000501613.1:p.Gln673His
ENST00000674652.1:c.*1829G>T	ENSP00000502620.1:n.*1829G>T
ENST00000674691.1:c.2040G>T	ENSP00000502247.1:p.Gln680His
ENST00000674768.1:c.*295G>T	ENSP00000501679.1:n.*295G>T
ENST00000674811.1:c.*233G>T	ENSP00000502055.1:n.*233G>T
ENST00000674848.1:n.2089G>T
ENST00000674962.1:n.2198G>T
ENST00000674963.1:c.2040G>T	ENSP00000501924.1:p.Gln680His
ENST00000675035.1:c.2040G>T	ENSP00000502712.1:p.Gln680His
ENST00000675045.1:c.2067G>T	ENSP00000502014.1:p.Gln689His
ENST00000675120.1:c.*350G>T	ENSP00000502823.1:n.*350G>T
ENST00000675133.1:c.2013G>T	ENSP00000502230.1:p.Gln671His
ENST00000675270.1:n.2175G>T
ENST00000675297.1:c.*392G>T	ENSP00000502753.1:n.*392G>T
ENST00000675371.1:c.1992+810G>T	ENSP00000502645.1:n.1992+810G>T
ENST00000675403.1:n.2960G>T
ENST00000675569.1:c.*1274G>T	ENSP00000502534.1:n.*1274G>T
ENST00000675643.1:c.2040G>T	ENSP00000502797.1:p.Gln680His
ENST00000675691.1:c.1911G>T	ENSP00000502196.1:p.Gln637His
ENST00000675751.1:c.*1067G>T	ENSP00000502277.1:n.*1067G>T
ENST00000675853.1:c.2040G>T	ENSP00000502367.1:p.Gln680His
ENST00000675917.1:n.2337G>T
ENST00000675953.1:c.1956G>T	ENSP00000502321.1:p.Gln652His
ENST00000675986.1:n.2198G>T
ENST00000676004.1:c.*2039G>T	ENSP00000502765.1:n.*2039G>T
ENST00000676040.1:c.*1274G>T	ENSP00000502108.1:n.*1274G>T
ENST00000676168.1:c.1992+810G>T	ENSP00000502479.1:n.1992+810G>T
ENST00000676209.1:c.*392G>T	ENSP00000502052.1:n.*392G>T
ENST00000676211.1:c.*1067G>T	ENSP00000502726.1:n.*1067G>T
ENST00000676212.1:c.2040G>T	ENSP00000501853.1:p.Gln680His
ENST00000676247.1:c.*392G>T	ENSP00000502699.1:n.*392G>T
ENST00000261772.12:c.2040G>T	ENSP00000261772.7:p.Gln680His
ENST00000564359.5:n.488+810G>T
ENST00000565361.2:c.385G>T
ENST00000569825.1:n.46G>T
NM_001605.2:c.2040G>T , LRG_359t1:c.2040G>T	NP_001596.2:p.Gln680His
XR_933220.1:n.2143+810G>T
XR_933220.3:n.2102+810G>T
NM_001605.3:c.2040G>T MANE Select	NP_001596.2:p.Gln680His