Canonical Allele Identifier: CA1697811373

Gene: GARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612355_30612357delinsATT , CM000669.2:g.30612355_30612357delinsATT	GRCh38
NC_000007.13:g.30651971_30651973delinsATT , CM000669.1:g.30651971_30651973delinsATT	GRCh37
NC_000007.12:g.30618496_30618498delinsATT	NCBI36
NG_007942.1:g.22791_22793delinsATT , LRG_243:g.22791_22793delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.1031+110_1031+112delinsATT MANE Select	ENSP00000373918.3:n.1031+110_1031+112delinsATT
ENST00000444666.6:c.1031+110_1031+112delinsATT	ENSP00000415447.2:n.1031+110_1031+112delinsATT
ENST00000470392.2:n.1121+110_1121+112delinsATT
ENST00000478124.6:n.1094+110_1094+112delinsATT
ENST00000485784.2:n.1110+110_1110+112delinsATT
ENST00000674616.1:c.*745+110_*745+112delinsATT	ENSP00000502408.1:n.*745+110_*745+112delinsATT
ENST00000674643.1:c.1031+110_1031+112delinsATT	ENSP00000501636.1:n.1031+110_1031+112delinsATT
ENST00000674734.1:n.1527+110_1527+112delinsATT
ENST00000674737.1:c.*369+110_*369+112delinsATT	ENSP00000502464.1:n.*369+110_*369+112delinsATT
ENST00000674807.1:c.1031+110_1031+112delinsATT	ENSP00000502814.1:n.1031+110_1031+112delinsATT
ENST00000674815.1:c.662+110_662+112delinsATT	ENSP00000502799.1:n.662+110_662+112delinsATT
ENST00000674851.1:c.662+110_662+112delinsATT	ENSP00000502451.1:n.662+110_662+112delinsATT
ENST00000674969.1:n.2904+110_2904+112delinsATT
ENST00000675051.1:c.830+110_830+112delinsATT	ENSP00000502296.1:n.830+110_830+112delinsATT
ENST00000675529.1:c.*901+110_*901+112delinsATT	ENSP00000501655.1:n.*901+110_*901+112delinsATT
ENST00000675587.1:n.1047+110_1047+112delinsATT
ENST00000675651.1:c.1031+110_1031+112delinsATT	ENSP00000502513.1:n.1031+110_1031+112delinsATT
ENST00000675693.1:c.863+110_863+112delinsATT	ENSP00000502174.1:n.863+110_863+112delinsATT
ENST00000675810.1:c.929+110_929+112delinsATT	ENSP00000502743.1:n.929+110_929+112delinsATT
ENST00000675859.1:c.1031+110_1031+112delinsATT	ENSP00000502033.1:n.1031+110_1031+112delinsATT
ENST00000675863.1:n.1039+110_1039+112delinsATT
ENST00000675886.1:n.7071+110_7071+112delinsATT
ENST00000676088.1:c.*973+110_*973+112delinsATT	ENSP00000501884.1:n.*973+110_*973+112delinsATT
ENST00000676140.1:c.1031+110_1031+112delinsATT	ENSP00000502571.1:n.1031+110_1031+112delinsATT
ENST00000676164.1:c.*482+110_*482+112delinsATT	ENSP00000501986.1:n.*482+110_*482+112delinsATT
ENST00000676210.1:c.*320+110_*320+112delinsATT	ENSP00000502373.1:n.*320+110_*320+112delinsATT
ENST00000676259.1:c.*463+110_*463+112delinsATT	ENSP00000501980.1:n.*463+110_*463+112delinsATT
ENST00000676403.1:c.1031+110_1031+112delinsATT	ENSP00000502681.1:n.1031+110_1031+112delinsATT
ENST00000389266.7:c.1031+110_1031+112delinsATT	ENSP00000373918.3:n.1031+110_1031+112delinsATT
ENST00000478124.5:n.1069+110_1069+112delinsATT
NM_001316772.1:c.869+110_869+112delinsATT	NP_001303701.1:n.869+110_869+112delinsATT
NM_002047.2:c.1031+110_1031+112delinsATT , LRG_243t1:c.1031+110_1031+112delinsATT	NP_002038.2:n.1031+110_1031+112delinsATT
NM_002047.3:c.1031+110_1031+112delinsATT	NP_002038.2:n.1031+110_1031+112delinsATT
XM_006715686.1:c.662+110_662+112delinsATT	XP_006715749.1:n.662+110_662+112delinsATT
XM_006715686.2:c.662+110_662+112delinsATT	XP_006715749.1:n.662+110_662+112delinsATT
NM_002047.4:c.1031+110_1031+112delinsATT MANE Select	NP_002038.2:n.1031+110_1031+112delinsATT