Canonical Allele Identifier: CA454246861

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30651721A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612105A>G , CM000669.2:g.30612105A>G	GRCh38
NC_000007.13:g.30651721A>G , CM000669.1:g.30651721A>G	GRCh37
NC_000007.12:g.30618246A>G	NCBI36
NG_007942.1:g.22541A>G , LRG_243:g.22541A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.891A>G MANE Select	ENSP00000373918.3:p.Arg297=
ENST00000444666.6:c.891A>G	ENSP00000415447.2:p.Arg297=
ENST00000470392.2:n.981A>G
ENST00000478124.6:n.954A>G
ENST00000485784.2:n.970A>G
ENST00000674616.1:c.*605A>G	ENSP00000502408.1:n.*605A>G
ENST00000674643.1:c.891A>G	ENSP00000501636.1:p.Arg297=
ENST00000674734.1:n.1387A>G
ENST00000674737.1:c.*229A>G	ENSP00000502464.1:n.*229A>G
ENST00000674807.1:c.891A>G	ENSP00000502814.1:p.Arg297=
ENST00000674815.1:c.522A>G	ENSP00000502799.1:p.Arg174=
ENST00000674851.1:c.522A>G	ENSP00000502451.1:p.Arg174=
ENST00000674969.1:n.2764A>G
ENST00000675051.1:c.690A>G	ENSP00000502296.1:p.Arg230=
ENST00000675529.1:c.*761A>G	ENSP00000501655.1:n.*761A>G
ENST00000675587.1:n.907A>G
ENST00000675651.1:c.891A>G	ENSP00000502513.1:p.Arg297=
ENST00000675693.1:c.723A>G	ENSP00000502174.1:p.Arg241=
ENST00000675810.1:c.789A>G	ENSP00000502743.1:p.Arg263=
ENST00000675859.1:c.891A>G	ENSP00000502033.1:p.Arg297=
ENST00000675863.1:n.899A>G
ENST00000675886.1:n.6931A>G
ENST00000676088.1:c.*833A>G	ENSP00000501884.1:n.*833A>G
ENST00000676140.1:c.891A>G	ENSP00000502571.1:p.Arg297=
ENST00000676164.1:c.*342A>G	ENSP00000501986.1:n.*342A>G
ENST00000676210.1:c.*180A>G	ENSP00000502373.1:n.*180A>G
ENST00000676259.1:c.*323A>G	ENSP00000501980.1:n.*323A>G
ENST00000676403.1:c.891A>G	ENSP00000502681.1:p.Arg297=
ENST00000389266.7:c.891A>G	ENSP00000373918.3:p.Arg297=
ENST00000478124.5:n.929A>G
NM_001316772.1:c.729A>G	NP_001303701.1:p.Arg243=
NM_002047.2:c.891A>G , LRG_243t1:c.891A>G	NP_002038.2:p.Arg297=
NM_002047.3:c.891A>G	NP_002038.2:p.Arg297=
XM_006715686.1:c.522A>G	XP_006715749.1:p.Arg174=
XM_006715686.2:c.522A>G	XP_006715749.1:p.Arg174=
NM_002047.4:c.891A>G MANE Select	NP_002038.2:p.Arg297=