Canonical Allele Identifier: CA1697778280

Gene: GARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30626384_30626386delinsCAG , CM000669.2:g.30626384_30626386delinsCAG	GRCh38
NC_000007.13:g.30666000_30666002delinsCAG , CM000669.1:g.30666000_30666002delinsCAG	GRCh37
NC_000007.12:g.30632525_30632527delinsCAG	NCBI36
NG_007942.1:g.36820_36822delinsCAG , LRG_243:g.36820_36822delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.1699+65_1699+67delinsCAG MANE Select	ENSP00000373918.3:n.1699+65_1699+67delinsCAG
ENST00000444666.6:c.1699+65_1699+67delinsCAG	ENSP00000415447.2:n.1699+65_1699+67delinsCAG
ENST00000470392.2:n.1789+65_1789+67delinsCAG
ENST00000485784.2:n.1778+65_1778+67delinsCAG
ENST00000674616.1:c.*1413+65_*1413+67delinsCAG	ENSP00000502408.1:n.*1413+65_*1413+67delinsCAG
ENST00000674643.1:c.*799+65_*799+67delinsCAG	ENSP00000501636.1:n.*799+65_*799+67delinsCAG
ENST00000674737.1:c.*1037+65_*1037+67delinsCAG	ENSP00000502464.1:n.*1037+65_*1037+67delinsCAG
ENST00000674807.1:c.1614-2176_1614-2174delinsCAG	ENSP00000502814.1:n.1614-2176_1614-2174delinsCAG
ENST00000674815.1:c.1330+65_1330+67delinsCAG	ENSP00000502799.1:n.1330+65_1330+67delinsCAG
ENST00000674851.1:c.1330+65_1330+67delinsCAG	ENSP00000502451.1:n.1330+65_1330+67delinsCAG
ENST00000674969.1:n.3572+65_3572+67delinsCAG
ENST00000675051.1:c.1498+65_1498+67delinsCAG	ENSP00000502296.1:n.1498+65_1498+67delinsCAG
ENST00000675529.1:c.*1569+65_*1569+67delinsCAG	ENSP00000501655.1:n.*1569+65_*1569+67delinsCAG
ENST00000675587.1:n.2531+65_2531+67delinsCAG
ENST00000675651.1:c.1699+65_1699+67delinsCAG	ENSP00000502513.1:n.1699+65_1699+67delinsCAG
ENST00000675693.1:c.1531+65_1531+67delinsCAG	ENSP00000502174.1:n.1531+65_1531+67delinsCAG
ENST00000675810.1:c.1597+65_1597+67delinsCAG	ENSP00000502743.1:n.1597+65_1597+67delinsCAG
ENST00000675859.1:c.1614-2176_1614-2174delinsCAG	ENSP00000502033.1:n.1614-2176_1614-2174delinsCAG
ENST00000675863.1:n.1707+65_1707+67delinsCAG
ENST00000675886.1:n.7739+65_7739+67delinsCAG
ENST00000676088.1:c.*1641+65_*1641+67delinsCAG	ENSP00000501884.1:n.*1641+65_*1641+67delinsCAG
ENST00000676140.1:c.*644+65_*644+67delinsCAG	ENSP00000502571.1:n.*644+65_*644+67delinsCAG
ENST00000676164.1:c.*1150+65_*1150+67delinsCAG	ENSP00000501986.1:n.*1150+65_*1150+67delinsCAG
ENST00000676210.1:c.*988+65_*988+67delinsCAG	ENSP00000502373.1:n.*988+65_*988+67delinsCAG
ENST00000676259.1:c.*1131+65_*1131+67delinsCAG	ENSP00000501980.1:n.*1131+65_*1131+67delinsCAG
ENST00000676403.1:c.1699+65_1699+67delinsCAG	ENSP00000502681.1:n.1699+65_1699+67delinsCAG
ENST00000389266.7:c.1699+65_1699+67delinsCAG	ENSP00000373918.3:n.1699+65_1699+67delinsCAG
ENST00000444666.5:c.220+65_220+67delinsCAG	ENSP00000415447.1:n.220+65_220+67delinsCAG
ENST00000470392.1:n.421+65_421+67delinsCAG
NM_001316772.1:c.1537+65_1537+67delinsCAG	NP_001303701.1:n.1537+65_1537+67delinsCAG
NM_002047.2:c.1699+65_1699+67delinsCAG , LRG_243t1:c.1699+65_1699+67delinsCAG	NP_002038.2:n.1699+65_1699+67delinsCAG
NM_002047.3:c.1699+65_1699+67delinsCAG	NP_002038.2:n.1699+65_1699+67delinsCAG
XM_006715686.1:c.1330+65_1330+67delinsCAG	XP_006715749.1:n.1330+65_1330+67delinsCAG
XM_006715686.2:c.1330+65_1330+67delinsCAG	XP_006715749.1:n.1330+65_1330+67delinsCAG
NM_002047.4:c.1699+65_1699+67delinsCAG MANE Select	NP_002038.2:n.1699+65_1699+67delinsCAG