Canonical Allele Identifier: CA1697811491

Gene: GARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612512_30612513delinsTC , CM000669.2:g.30612512_30612513delinsTC	GRCh38
NC_000007.13:g.30652128_30652129delinsTC , CM000669.1:g.30652128_30652129delinsTC	GRCh37
NC_000007.12:g.30618653_30618654delinsTC	NCBI36
NG_007942.1:g.22948_22949delinsTC , LRG_243:g.22948_22949delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.1031+267_1031+268delinsTC MANE Select	ENSP00000373918.3:n.1031+267_1031+268delinsTC
ENST00000444666.6:c.1031+267_1031+268delinsTC	ENSP00000415447.2:n.1031+267_1031+268delinsTC
ENST00000470392.2:n.1121+267_1121+268delinsTC
ENST00000478124.6:n.1094+267_1094+268delinsTC
ENST00000485784.2:n.1110+267_1110+268delinsTC
ENST00000674616.1:c.*745+267_*745+268delinsTC	ENSP00000502408.1:n.*745+267_*745+268delinsTC
ENST00000674643.1:c.1031+267_1031+268delinsTC	ENSP00000501636.1:n.1031+267_1031+268delinsTC
ENST00000674734.1:n.1527+267_1527+268delinsTC
ENST00000674737.1:c.*369+267_*369+268delinsTC	ENSP00000502464.1:n.*369+267_*369+268delinsTC
ENST00000674807.1:c.1031+267_1031+268delinsTC	ENSP00000502814.1:n.1031+267_1031+268delinsTC
ENST00000674815.1:c.662+267_662+268delinsTC	ENSP00000502799.1:n.662+267_662+268delinsTC
ENST00000674851.1:c.662+267_662+268delinsTC	ENSP00000502451.1:n.662+267_662+268delinsTC
ENST00000674969.1:n.2904+267_2904+268delinsTC
ENST00000675051.1:c.830+267_830+268delinsTC	ENSP00000502296.1:n.830+267_830+268delinsTC
ENST00000675529.1:c.*901+267_*901+268delinsTC	ENSP00000501655.1:n.*901+267_*901+268delinsTC
ENST00000675587.1:n.1047+267_1047+268delinsTC
ENST00000675651.1:c.1031+267_1031+268delinsTC	ENSP00000502513.1:n.1031+267_1031+268delinsTC
ENST00000675693.1:c.863+267_863+268delinsTC	ENSP00000502174.1:n.863+267_863+268delinsTC
ENST00000675810.1:c.929+267_929+268delinsTC	ENSP00000502743.1:n.929+267_929+268delinsTC
ENST00000675859.1:c.1031+267_1031+268delinsTC	ENSP00000502033.1:n.1031+267_1031+268delinsTC
ENST00000675863.1:n.1039+267_1039+268delinsTC
ENST00000675886.1:n.7071+267_7071+268delinsTC
ENST00000676088.1:c.*973+267_*973+268delinsTC	ENSP00000501884.1:n.*973+267_*973+268delinsTC
ENST00000676140.1:c.1031+267_1031+268delinsTC	ENSP00000502571.1:n.1031+267_1031+268delinsTC
ENST00000676164.1:c.*482+267_*482+268delinsTC	ENSP00000501986.1:n.*482+267_*482+268delinsTC
ENST00000676210.1:c.*320+267_*320+268delinsTC	ENSP00000502373.1:n.*320+267_*320+268delinsTC
ENST00000676259.1:c.*463+267_*463+268delinsTC	ENSP00000501980.1:n.*463+267_*463+268delinsTC
ENST00000676403.1:c.1031+267_1031+268delinsTC	ENSP00000502681.1:n.1031+267_1031+268delinsTC
ENST00000389266.7:c.1031+267_1031+268delinsTC	ENSP00000373918.3:n.1031+267_1031+268delinsTC
ENST00000478124.5:n.1069+267_1069+268delinsTC
NM_001316772.1:c.869+267_869+268delinsTC	NP_001303701.1:n.869+267_869+268delinsTC
NM_002047.2:c.1031+267_1031+268delinsTC , LRG_243t1:c.1031+267_1031+268delinsTC	NP_002038.2:n.1031+267_1031+268delinsTC
NM_002047.3:c.1031+267_1031+268delinsTC	NP_002038.2:n.1031+267_1031+268delinsTC
XM_006715686.1:c.662+267_662+268delinsTC	XP_006715749.1:n.662+267_662+268delinsTC
XM_006715686.2:c.662+267_662+268delinsTC	XP_006715749.1:n.662+267_662+268delinsTC
NM_002047.4:c.1031+267_1031+268delinsTC MANE Select	NP_002038.2:n.1031+267_1031+268delinsTC