Canonical Allele Identifier: CA367124969

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30651759G>C (hg19) ; chr7:g.30612143G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612143G>C , CM000669.2:g.30612143G>C	GRCh38
NC_000007.13:g.30651759G>C , CM000669.1:g.30651759G>C	GRCh37
NC_000007.12:g.30618284G>C	NCBI36
NG_007942.1:g.22579G>C , LRG_243:g.22579G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.929G>C MANE Select	ENSP00000373918.3:p.Arg310Pro
ENST00000444666.6:c.929G>C	ENSP00000415447.2:p.Arg310Pro
ENST00000470392.2:n.1019G>C
ENST00000478124.6:n.992G>C
ENST00000485784.2:n.1008G>C
ENST00000674616.1:c.*643G>C	ENSP00000502408.1:n.*643G>C
ENST00000674643.1:c.929G>C	ENSP00000501636.1:p.Arg310Pro
ENST00000674734.1:n.1425G>C
ENST00000674737.1:c.*267G>C	ENSP00000502464.1:n.*267G>C
ENST00000674807.1:c.929G>C	ENSP00000502814.1:p.Arg310Pro
ENST00000674815.1:c.560G>C	ENSP00000502799.1:p.Arg187Pro
ENST00000674851.1:c.560G>C	ENSP00000502451.1:p.Arg187Pro
ENST00000674969.1:n.2802G>C
ENST00000675051.1:c.728G>C	ENSP00000502296.1:p.Arg243Pro
ENST00000675529.1:c.*799G>C	ENSP00000501655.1:n.*799G>C
ENST00000675587.1:n.945G>C
ENST00000675651.1:c.929G>C	ENSP00000502513.1:p.Arg310Pro
ENST00000675693.1:c.761G>C	ENSP00000502174.1:p.Arg254Pro
ENST00000675810.1:c.827G>C	ENSP00000502743.1:p.Arg276Pro
ENST00000675859.1:c.929G>C	ENSP00000502033.1:p.Arg310Pro
ENST00000675863.1:n.937G>C
ENST00000675886.1:n.6969G>C
ENST00000676088.1:c.*871G>C	ENSP00000501884.1:n.*871G>C
ENST00000676140.1:c.929G>C	ENSP00000502571.1:p.Arg310Pro
ENST00000676164.1:c.*380G>C	ENSP00000501986.1:n.*380G>C
ENST00000676210.1:c.*218G>C	ENSP00000502373.1:n.*218G>C
ENST00000676259.1:c.*361G>C	ENSP00000501980.1:n.*361G>C
ENST00000676403.1:c.929G>C	ENSP00000502681.1:p.Arg310Pro
ENST00000389266.7:c.929G>C	ENSP00000373918.3:p.Arg310Pro
ENST00000478124.5:n.967G>C
NM_001316772.1:c.767G>C	NP_001303701.1:p.Arg256Pro
NM_002047.2:c.929G>C , LRG_243t1:c.929G>C	NP_002038.2:p.Arg310Pro
NM_002047.3:c.929G>C	NP_002038.2:p.Arg310Pro
XM_006715686.1:c.560G>C	XP_006715749.1:p.Arg187Pro
XM_006715686.2:c.560G>C	XP_006715749.1:p.Arg187Pro
NM_002047.4:c.929G>C MANE Select	NP_002038.2:p.Arg310Pro