Canonical Allele Identifier: CA1697777661

Gene: GARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30626105_30626108delinsCTTA , CM000669.2:g.30626105_30626108delinsCTTA	GRCh38
NC_000007.13:g.30665721_30665724delinsCTTA , CM000669.1:g.30665721_30665724delinsCTTA	GRCh37
NC_000007.12:g.30632246_30632249delinsCTTA	NCBI36
NG_007942.1:g.36541_36544delinsCTTA , LRG_243:g.36541_36544delinsCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.1614-129_1614-126delinsCTTA MANE Select	ENSP00000373918.3:n.1614-129_1614-126delinsCTTA
ENST00000444666.6:c.1614-129_1614-126delinsCTTA	ENSP00000415447.2:n.1614-129_1614-126delinsCTTA
ENST00000470392.2:n.1704-129_1704-126delinsCTTA
ENST00000485784.2:n.1693-129_1693-126delinsCTTA
ENST00000674616.1:c.*1328-129_*1328-126delinsCTTA	ENSP00000502408.1:n.*1328-129_*1328-126delinsCTTA
ENST00000674643.1:c.*714-129_*714-126delinsCTTA	ENSP00000501636.1:n.*714-129_*714-126delinsCTTA
ENST00000674737.1:c.*952-129_*952-126delinsCTTA	ENSP00000502464.1:n.*952-129_*952-126delinsCTTA
ENST00000674807.1:c.1614-2455_1614-2452delinsCTTA	ENSP00000502814.1:n.1614-2455_1614-2452delinsCTTA
ENST00000674815.1:c.1245-129_1245-126delinsCTTA	ENSP00000502799.1:n.1245-129_1245-126delinsCTTA
ENST00000674851.1:c.1245-129_1245-126delinsCTTA	ENSP00000502451.1:n.1245-129_1245-126delinsCTTA
ENST00000674969.1:n.3487-129_3487-126delinsCTTA
ENST00000675051.1:c.1413-129_1413-126delinsCTTA	ENSP00000502296.1:n.1413-129_1413-126delinsCTTA
ENST00000675529.1:c.*1484-129_*1484-126delinsCTTA	ENSP00000501655.1:n.*1484-129_*1484-126delinsCTTA
ENST00000675587.1:n.2446-129_2446-126delinsCTTA
ENST00000675651.1:c.1614-129_1614-126delinsCTTA	ENSP00000502513.1:n.1614-129_1614-126delinsCTTA
ENST00000675693.1:c.1446-129_1446-126delinsCTTA	ENSP00000502174.1:n.1446-129_1446-126delinsCTTA
ENST00000675810.1:c.1512-129_1512-126delinsCTTA	ENSP00000502743.1:n.1512-129_1512-126delinsCTTA
ENST00000675859.1:c.1614-2455_1614-2452delinsCTTA	ENSP00000502033.1:n.1614-2455_1614-2452delinsCTTA
ENST00000675863.1:n.1622-129_1622-126delinsCTTA
ENST00000675886.1:n.7654-129_7654-126delinsCTTA
ENST00000676088.1:c.*1556-129_*1556-126delinsCTTA	ENSP00000501884.1:n.*1556-129_*1556-126delinsCTTA
ENST00000676140.1:c.*559-129_*559-126delinsCTTA	ENSP00000502571.1:n.*559-129_*559-126delinsCTTA
ENST00000676164.1:c.*1065-129_*1065-126delinsCTTA	ENSP00000501986.1:n.*1065-129_*1065-126delinsCTTA
ENST00000676210.1:c.*903-129_*903-126delinsCTTA	ENSP00000502373.1:n.*903-129_*903-126delinsCTTA
ENST00000676259.1:c.*1046-129_*1046-126delinsCTTA	ENSP00000501980.1:n.*1046-129_*1046-126delinsCTTA
ENST00000676403.1:c.1614-129_1614-126delinsCTTA	ENSP00000502681.1:n.1614-129_1614-126delinsCTTA
ENST00000389266.7:c.1614-129_1614-126delinsCTTA	ENSP00000373918.3:n.1614-129_1614-126delinsCTTA
ENST00000444666.5:c.135-129_135-126delinsCTTA	ENSP00000415447.1:n.135-129_135-126delinsCTTA
ENST00000470392.1:n.336-129_336-126delinsCTTA
NM_001316772.1:c.1452-129_1452-126delinsCTTA	NP_001303701.1:n.1452-129_1452-126delinsCTTA
NM_002047.2:c.1614-129_1614-126delinsCTTA , LRG_243t1:c.1614-129_1614-126delinsCTTA	NP_002038.2:n.1614-129_1614-126delinsCTTA
NM_002047.3:c.1614-129_1614-126delinsCTTA	NP_002038.2:n.1614-129_1614-126delinsCTTA
XM_006715686.1:c.1245-129_1245-126delinsCTTA	XP_006715749.1:n.1245-129_1245-126delinsCTTA
XM_006715686.2:c.1245-129_1245-126delinsCTTA	XP_006715749.1:n.1245-129_1245-126delinsCTTA
NM_002047.4:c.1614-129_1614-126delinsCTTA MANE Select	NP_002038.2:n.1614-129_1614-126delinsCTTA