Canonical Allele Identifier: CA367124412

Gene: GARS1

Linked Data

• dbSNP Id: rs1584032237
• MyVariant Identifiers: chr7:g.30649270G>A (hg19) ; chr7:g.30609654G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30609654G>A , CM000669.2:g.30609654G>A	GRCh38
NC_000007.13:g.30649270G>A , CM000669.1:g.30649270G>A	GRCh37
NC_000007.12:g.30615795G>A	NCBI36
NG_007942.1:g.20090G>A , LRG_243:g.20090G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.805G>A MANE Select	ENSP00000373918.3:p.Gly269Arg
ENST00000444666.6:c.805G>A	ENSP00000415447.2:p.Gly269Arg
ENST00000470392.2:n.895G>A
ENST00000478124.6:n.868G>A
ENST00000485784.2:n.884G>A
ENST00000674616.1:c.*519G>A	ENSP00000502408.1:n.*519G>A
ENST00000674643.1:c.805G>A	ENSP00000501636.1:p.Gly269Arg
ENST00000674734.1:n.1301G>A
ENST00000674737.1:c.*143G>A	ENSP00000502464.1:n.*143G>A
ENST00000674807.1:c.805G>A	ENSP00000502814.1:p.Gly269Arg
ENST00000674815.1:c.436G>A	ENSP00000502799.1:p.Gly146Arg
ENST00000674851.1:c.436G>A	ENSP00000502451.1:p.Gly146Arg
ENST00000674969.1:n.2678G>A
ENST00000675051.1:c.604G>A	ENSP00000502296.1:p.Gly202Arg
ENST00000675529.1:c.*675G>A	ENSP00000501655.1:n.*675G>A
ENST00000675587.1:n.821G>A
ENST00000675651.1:c.805G>A	ENSP00000502513.1:p.Gly269Arg
ENST00000675693.1:c.637G>A	ENSP00000502174.1:p.Gly213Arg
ENST00000675810.1:c.703G>A	ENSP00000502743.1:p.Gly235Arg
ENST00000675859.1:c.805G>A	ENSP00000502033.1:p.Gly269Arg
ENST00000675863.1:n.813G>A
ENST00000675886.1:n.6845G>A
ENST00000676088.1:c.*747G>A	ENSP00000501884.1:n.*747G>A
ENST00000676140.1:c.805G>A	ENSP00000502571.1:p.Gly269Arg
ENST00000676164.1:c.*256G>A	ENSP00000501986.1:n.*256G>A
ENST00000676210.1:c.*94G>A	ENSP00000502373.1:n.*94G>A
ENST00000676259.1:c.*237G>A	ENSP00000501980.1:n.*237G>A
ENST00000676403.1:c.805G>A	ENSP00000502681.1:p.Gly269Arg
ENST00000389266.7:c.805G>A	ENSP00000373918.3:p.Gly269Arg
ENST00000478124.5:n.843G>A
NM_001316772.1:c.643G>A	NP_001303701.1:p.Gly215Arg
NM_002047.2:c.805G>A , LRG_243t1:c.805G>A	NP_002038.2:p.Gly269Arg
NM_002047.3:c.805G>A	NP_002038.2:p.Gly269Arg
XM_006715686.1:c.436G>A	XP_006715749.1:p.Gly146Arg
XM_006715686.2:c.436G>A	XP_006715749.1:p.Gly146Arg
NM_002047.4:c.805G>A MANE Select	NP_002038.2:p.Gly269Arg