Canonical Allele Identifier: CA396557544

Gene: AARS1

Linked Data

• MyVariant Identifiers: chr16:g.70291955C>A (hg19) ; chr16:g.70258052C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70258052C>A , CM000678.2:g.70258052C>A	GRCh38
NC_000016.9:g.70291955C>A , CM000678.1:g.70291955C>A	GRCh37
NC_000016.8:g.68849456C>A	NCBI36
NG_023191.1:g.36458G>T , LRG_359:g.36458G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261772.13:c.2158G>T MANE Select	ENSP00000261772.8:p.Val720Phe
ENST00000564359.6:n.2150+928G>T
ENST00000565361.3:c.2158G>T	ENSP00000455360.3:p.Val720Phe
ENST00000674512.1:c.2137G>T	ENSP00000501613.1:p.Val713Phe
ENST00000674652.1:c.*1947G>T	ENSP00000502620.1:n.*1947G>T
ENST00000674691.1:c.2158G>T	ENSP00000502247.1:p.Val720Phe
ENST00000674768.1:c.*413G>T	ENSP00000501679.1:n.*413G>T
ENST00000674811.1:c.*351G>T	ENSP00000502055.1:n.*351G>T
ENST00000674848.1:n.2207G>T
ENST00000674962.1:n.2316G>T
ENST00000674963.1:c.2158G>T	ENSP00000501924.1:p.Val720Phe
ENST00000675035.1:c.2157+1G>T	ENSP00000502712.1:n.2157+1G>T
ENST00000675045.1:c.2185G>T	ENSP00000502014.1:p.Val729Phe
ENST00000675120.1:c.*468G>T	ENSP00000502823.1:n.*468G>T
ENST00000675133.1:c.2131G>T	ENSP00000502230.1:p.Val711Phe
ENST00000675270.1:n.2293G>T
ENST00000675297.1:c.*510G>T	ENSP00000502753.1:n.*510G>T
ENST00000675371.1:c.1992+928G>T	ENSP00000502645.1:n.1992+928G>T
ENST00000675403.1:n.3078G>T
ENST00000675569.1:c.*1392G>T	ENSP00000502534.1:n.*1392G>T
ENST00000675643.1:c.2158G>T	ENSP00000502797.1:p.Val720Phe
ENST00000675691.1:c.2029G>T	ENSP00000502196.1:p.Val677Phe
ENST00000675751.1:c.*1185G>T	ENSP00000502277.1:n.*1185G>T
ENST00000675853.1:c.2158G>T	ENSP00000502367.1:p.Val720Phe
ENST00000675917.1:n.2455G>T
ENST00000675953.1:c.2074G>T	ENSP00000502321.1:p.Val692Phe
ENST00000675986.1:n.2316G>T
ENST00000676004.1:c.*2157G>T	ENSP00000502765.1:n.*2157G>T
ENST00000676040.1:c.*1392G>T	ENSP00000502108.1:n.*1392G>T
ENST00000676168.1:c.1992+928G>T	ENSP00000502479.1:n.1992+928G>T
ENST00000676209.1:c.*510G>T	ENSP00000502052.1:n.*510G>T
ENST00000676211.1:c.*1185G>T	ENSP00000502726.1:n.*1185G>T
ENST00000676212.1:c.2158G>T	ENSP00000501853.1:p.Val720Phe
ENST00000676247.1:c.*510G>T	ENSP00000502699.1:n.*510G>T
ENST00000261772.12:c.2158G>T	ENSP00000261772.7:p.Val720Phe
ENST00000564359.5:n.488+928G>T
ENST00000565361.2:c.503G>T
ENST00000569825.1:n.164G>T
NM_001605.2:c.2158G>T , LRG_359t1:c.2158G>T	NP_001596.2:p.Val720Phe
XR_933220.1:n.2143+928G>T
XR_933220.3:n.2102+928G>T
NM_001605.3:c.2158G>T MANE Select	NP_001596.2:p.Val720Phe