Canonical Allele Identifier: CA1697811378

Gene: GARS1

Linked Data

• dbSNP Id: rs1782777345
• gnomAD v4: 7-30612355-ATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612359_30612360del , CM000669.2:g.30612359_30612360del	GRCh38
NC_000007.13:g.30651975_30651976del , CM000669.1:g.30651975_30651976del	GRCh37
NC_000007.12:g.30618500_30618501del	NCBI36
NG_007942.1:g.22795_22796del , LRG_243:g.22795_22796del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.1031+114_1031+115del MANE Select	ENSP00000373918.3:n.1031+114_1031+115del
ENST00000444666.6:c.1031+114_1031+115del	ENSP00000415447.2:n.1031+114_1031+115del
ENST00000470392.2:n.1121+114_1121+115del
ENST00000478124.6:n.1094+114_1094+115del
ENST00000485784.2:n.1110+114_1110+115del
ENST00000674616.1:c.*745+114_*745+115del	ENSP00000502408.1:n.*745+114_*745+115del
ENST00000674643.1:c.1031+114_1031+115del	ENSP00000501636.1:n.1031+114_1031+115del
ENST00000674734.1:n.1527+114_1527+115del
ENST00000674737.1:c.*369+114_*369+115del	ENSP00000502464.1:n.*369+114_*369+115del
ENST00000674807.1:c.1031+114_1031+115del	ENSP00000502814.1:n.1031+114_1031+115del
ENST00000674815.1:c.662+114_662+115del	ENSP00000502799.1:n.662+114_662+115del
ENST00000674851.1:c.662+114_662+115del	ENSP00000502451.1:n.662+114_662+115del
ENST00000674969.1:n.2904+114_2904+115del
ENST00000675051.1:c.830+114_830+115del	ENSP00000502296.1:n.830+114_830+115del
ENST00000675529.1:c.*901+114_*901+115del	ENSP00000501655.1:n.*901+114_*901+115del
ENST00000675587.1:n.1047+114_1047+115del
ENST00000675651.1:c.1031+114_1031+115del	ENSP00000502513.1:n.1031+114_1031+115del
ENST00000675693.1:c.863+114_863+115del	ENSP00000502174.1:n.863+114_863+115del
ENST00000675810.1:c.929+114_929+115del	ENSP00000502743.1:n.929+114_929+115del
ENST00000675859.1:c.1031+114_1031+115del	ENSP00000502033.1:n.1031+114_1031+115del
ENST00000675863.1:n.1039+114_1039+115del
ENST00000675886.1:n.7071+114_7071+115del
ENST00000676088.1:c.*973+114_*973+115del	ENSP00000501884.1:n.*973+114_*973+115del
ENST00000676140.1:c.1031+114_1031+115del	ENSP00000502571.1:n.1031+114_1031+115del
ENST00000676164.1:c.*482+114_*482+115del	ENSP00000501986.1:n.*482+114_*482+115del
ENST00000676210.1:c.*320+114_*320+115del	ENSP00000502373.1:n.*320+114_*320+115del
ENST00000676259.1:c.*463+114_*463+115del	ENSP00000501980.1:n.*463+114_*463+115del
ENST00000676403.1:c.1031+114_1031+115del	ENSP00000502681.1:n.1031+114_1031+115del
ENST00000389266.7:c.1031+114_1031+115del	ENSP00000373918.3:n.1031+114_1031+115del
ENST00000478124.5:n.1069+114_1069+115del
NM_001316772.1:c.869+114_869+115del	NP_001303701.1:n.869+114_869+115del
NM_002047.2:c.1031+114_1031+115del , LRG_243t1:c.1031+114_1031+115del	NP_002038.2:n.1031+114_1031+115del
NM_002047.3:c.1031+114_1031+115del	NP_002038.2:n.1031+114_1031+115del
XM_006715686.1:c.662+114_662+115del	XP_006715749.1:n.662+114_662+115del
XM_006715686.2:c.662+114_662+115del	XP_006715749.1:n.662+114_662+115del
NM_002047.4:c.1031+114_1031+115del MANE Select	NP_002038.2:n.1031+114_1031+115del