Canonical Allele Identifier: CA396557698

Gene: AARS1

Linked Data

• MyVariant Identifiers: chr16:g.70292037G>C (hg19) ; chr16:g.70258134G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70258134G>C , CM000678.2:g.70258134G>C	GRCh38
NC_000016.9:g.70292037G>C , CM000678.1:g.70292037G>C	GRCh37
NC_000016.8:g.68849538G>C	NCBI36
NG_023191.1:g.36376C>G , LRG_359:g.36376C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261772.13:c.2076C>G MANE Select	ENSP00000261772.8:p.Asp692Glu
ENST00000564359.6:n.2150+846C>G
ENST00000565361.3:c.2076C>G	ENSP00000455360.3:p.Asp692Glu
ENST00000674512.1:c.2055C>G	ENSP00000501613.1:p.Asp685Glu
ENST00000674652.1:c.*1865C>G	ENSP00000502620.1:n.*1865C>G
ENST00000674691.1:c.2076C>G	ENSP00000502247.1:p.Asp692Glu
ENST00000674768.1:c.*331C>G	ENSP00000501679.1:n.*331C>G
ENST00000674811.1:c.*269C>G	ENSP00000502055.1:n.*269C>G
ENST00000674848.1:n.2125C>G
ENST00000674962.1:n.2234C>G
ENST00000674963.1:c.2076C>G	ENSP00000501924.1:p.Asp692Glu
ENST00000675035.1:c.2076C>G	ENSP00000502712.1:p.Asp692Glu
ENST00000675045.1:c.2103C>G	ENSP00000502014.1:p.Asp701Glu
ENST00000675120.1:c.*386C>G	ENSP00000502823.1:n.*386C>G
ENST00000675133.1:c.2049C>G	ENSP00000502230.1:p.Asp683Glu
ENST00000675270.1:n.2211C>G
ENST00000675297.1:c.*428C>G	ENSP00000502753.1:n.*428C>G
ENST00000675371.1:c.1992+846C>G	ENSP00000502645.1:n.1992+846C>G
ENST00000675403.1:n.2996C>G
ENST00000675569.1:c.*1310C>G	ENSP00000502534.1:n.*1310C>G
ENST00000675643.1:c.2076C>G	ENSP00000502797.1:p.Asp692Glu
ENST00000675691.1:c.1947C>G	ENSP00000502196.1:p.Asp649Glu
ENST00000675751.1:c.*1103C>G	ENSP00000502277.1:n.*1103C>G
ENST00000675853.1:c.2076C>G	ENSP00000502367.1:p.Asp692Glu
ENST00000675917.1:n.2373C>G
ENST00000675953.1:c.1992C>G	ENSP00000502321.1:p.Asp664Glu
ENST00000675986.1:n.2234C>G
ENST00000676004.1:c.*2075C>G	ENSP00000502765.1:n.*2075C>G
ENST00000676040.1:c.*1310C>G	ENSP00000502108.1:n.*1310C>G
ENST00000676168.1:c.1992+846C>G	ENSP00000502479.1:n.1992+846C>G
ENST00000676209.1:c.*428C>G	ENSP00000502052.1:n.*428C>G
ENST00000676211.1:c.*1103C>G	ENSP00000502726.1:n.*1103C>G
ENST00000676212.1:c.2076C>G	ENSP00000501853.1:p.Asp692Glu
ENST00000676247.1:c.*428C>G	ENSP00000502699.1:n.*428C>G
ENST00000261772.12:c.2076C>G	ENSP00000261772.7:p.Asp692Glu
ENST00000564359.5:n.488+846C>G
ENST00000565361.2:c.421C>G
ENST00000569825.1:n.82C>G
NM_001605.2:c.2076C>G , LRG_359t1:c.2076C>G	NP_001596.2:p.Asp692Glu
XR_933220.1:n.2143+846C>G
XR_933220.3:n.2102+846C>G
NM_001605.3:c.2076C>G MANE Select	NP_001596.2:p.Asp692Glu