Canonical Allele Identifier: CA1697811476

Gene: GARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612485_30612486delinsGT , CM000669.2:g.30612485_30612486delinsGT	GRCh38
NC_000007.13:g.30652101_30652102delinsGT , CM000669.1:g.30652101_30652102delinsGT	GRCh37
NC_000007.12:g.30618626_30618627delinsGT	NCBI36
NG_007942.1:g.22921_22922delinsGT , LRG_243:g.22921_22922delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.1031+240_1031+241delinsGT MANE Select	ENSP00000373918.3:n.1031+240_1031+241delinsGT
ENST00000444666.6:c.1031+240_1031+241delinsGT	ENSP00000415447.2:n.1031+240_1031+241delinsGT
ENST00000470392.2:n.1121+240_1121+241delinsGT
ENST00000478124.6:n.1094+240_1094+241delinsGT
ENST00000485784.2:n.1110+240_1110+241delinsGT
ENST00000674616.1:c.*745+240_*745+241delinsGT	ENSP00000502408.1:n.*745+240_*745+241delinsGT
ENST00000674643.1:c.1031+240_1031+241delinsGT	ENSP00000501636.1:n.1031+240_1031+241delinsGT
ENST00000674734.1:n.1527+240_1527+241delinsGT
ENST00000674737.1:c.*369+240_*369+241delinsGT	ENSP00000502464.1:n.*369+240_*369+241delinsGT
ENST00000674807.1:c.1031+240_1031+241delinsGT	ENSP00000502814.1:n.1031+240_1031+241delinsGT
ENST00000674815.1:c.662+240_662+241delinsGT	ENSP00000502799.1:n.662+240_662+241delinsGT
ENST00000674851.1:c.662+240_662+241delinsGT	ENSP00000502451.1:n.662+240_662+241delinsGT
ENST00000674969.1:n.2904+240_2904+241delinsGT
ENST00000675051.1:c.830+240_830+241delinsGT	ENSP00000502296.1:n.830+240_830+241delinsGT
ENST00000675529.1:c.*901+240_*901+241delinsGT	ENSP00000501655.1:n.*901+240_*901+241delinsGT
ENST00000675587.1:n.1047+240_1047+241delinsGT
ENST00000675651.1:c.1031+240_1031+241delinsGT	ENSP00000502513.1:n.1031+240_1031+241delinsGT
ENST00000675693.1:c.863+240_863+241delinsGT	ENSP00000502174.1:n.863+240_863+241delinsGT
ENST00000675810.1:c.929+240_929+241delinsGT	ENSP00000502743.1:n.929+240_929+241delinsGT
ENST00000675859.1:c.1031+240_1031+241delinsGT	ENSP00000502033.1:n.1031+240_1031+241delinsGT
ENST00000675863.1:n.1039+240_1039+241delinsGT
ENST00000675886.1:n.7071+240_7071+241delinsGT
ENST00000676088.1:c.*973+240_*973+241delinsGT	ENSP00000501884.1:n.*973+240_*973+241delinsGT
ENST00000676140.1:c.1031+240_1031+241delinsGT	ENSP00000502571.1:n.1031+240_1031+241delinsGT
ENST00000676164.1:c.*482+240_*482+241delinsGT	ENSP00000501986.1:n.*482+240_*482+241delinsGT
ENST00000676210.1:c.*320+240_*320+241delinsGT	ENSP00000502373.1:n.*320+240_*320+241delinsGT
ENST00000676259.1:c.*463+240_*463+241delinsGT	ENSP00000501980.1:n.*463+240_*463+241delinsGT
ENST00000676403.1:c.1031+240_1031+241delinsGT	ENSP00000502681.1:n.1031+240_1031+241delinsGT
ENST00000389266.7:c.1031+240_1031+241delinsGT	ENSP00000373918.3:n.1031+240_1031+241delinsGT
ENST00000478124.5:n.1069+240_1069+241delinsGT
NM_001316772.1:c.869+240_869+241delinsGT	NP_001303701.1:n.869+240_869+241delinsGT
NM_002047.2:c.1031+240_1031+241delinsGT , LRG_243t1:c.1031+240_1031+241delinsGT	NP_002038.2:n.1031+240_1031+241delinsGT
NM_002047.3:c.1031+240_1031+241delinsGT	NP_002038.2:n.1031+240_1031+241delinsGT
XM_006715686.1:c.662+240_662+241delinsGT	XP_006715749.1:n.662+240_662+241delinsGT
XM_006715686.2:c.662+240_662+241delinsGT	XP_006715749.1:n.662+240_662+241delinsGT
NM_002047.4:c.1031+240_1031+241delinsGT MANE Select	NP_002038.2:n.1031+240_1031+241delinsGT