Canonical Allele Identifier: CA454246832

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30649317T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30609701T>C , CM000669.2:g.30609701T>C	GRCh38
NC_000007.13:g.30649317T>C , CM000669.1:g.30649317T>C	GRCh37
NC_000007.12:g.30615842T>C	NCBI36
NG_007942.1:g.20137T>C , LRG_243:g.20137T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.852T>C MANE Select	ENSP00000373918.3:p.Thr284=
ENST00000444666.6:c.852T>C	ENSP00000415447.2:p.Thr284=
ENST00000470392.2:n.942T>C
ENST00000478124.6:n.915T>C
ENST00000485784.2:n.931T>C
ENST00000674616.1:c.*566T>C	ENSP00000502408.1:n.*566T>C
ENST00000674643.1:c.852T>C	ENSP00000501636.1:p.Thr284=
ENST00000674734.1:n.1348T>C
ENST00000674737.1:c.*190T>C	ENSP00000502464.1:n.*190T>C
ENST00000674807.1:c.852T>C	ENSP00000502814.1:p.Thr284=
ENST00000674815.1:c.483T>C	ENSP00000502799.1:p.Thr161=
ENST00000674851.1:c.483T>C	ENSP00000502451.1:p.Thr161=
ENST00000674969.1:n.2725T>C
ENST00000675051.1:c.651T>C	ENSP00000502296.1:p.Thr217=
ENST00000675529.1:c.*722T>C	ENSP00000501655.1:n.*722T>C
ENST00000675587.1:n.868T>C
ENST00000675651.1:c.852T>C	ENSP00000502513.1:p.Thr284=
ENST00000675693.1:c.684T>C	ENSP00000502174.1:p.Thr228=
ENST00000675810.1:c.750T>C	ENSP00000502743.1:p.Thr250=
ENST00000675859.1:c.852T>C	ENSP00000502033.1:p.Thr284=
ENST00000675863.1:n.860T>C
ENST00000675886.1:n.6892T>C
ENST00000676088.1:c.*794T>C	ENSP00000501884.1:n.*794T>C
ENST00000676140.1:c.852T>C	ENSP00000502571.1:p.Thr284=
ENST00000676164.1:c.*303T>C	ENSP00000501986.1:n.*303T>C
ENST00000676210.1:c.*141T>C	ENSP00000502373.1:n.*141T>C
ENST00000676259.1:c.*284T>C	ENSP00000501980.1:n.*284T>C
ENST00000676403.1:c.852T>C	ENSP00000502681.1:p.Thr284=
ENST00000389266.7:c.852T>C	ENSP00000373918.3:p.Thr284=
ENST00000478124.5:n.890T>C
NM_001316772.1:c.690T>C	NP_001303701.1:p.Thr230=
NM_002047.2:c.852T>C , LRG_243t1:c.852T>C	NP_002038.2:p.Thr284=
NM_002047.3:c.852T>C	NP_002038.2:p.Thr284=
XM_006715686.1:c.483T>C	XP_006715749.1:p.Thr161=
XM_006715686.2:c.483T>C	XP_006715749.1:p.Thr161=
NM_002047.4:c.852T>C MANE Select	NP_002038.2:p.Thr284=