Canonical Allele Identifier: CA1697778338
Gene: GARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30626401_30626402delinsAC , CM000669.2:g.30626401_30626402delinsAC GRCh38
NC_000007.13:g.30666017_30666018delinsAC , CM000669.1:g.30666017_30666018delinsAC GRCh37
NC_000007.12:g.30632542_30632543delinsAC NCBI36
NG_007942.1:g.36837_36838delinsAC , LRG_243:g.36837_36838delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000389266.8:c.1699+82_1699+83delinsAC MANE Select ENSP00000373918.3:n.1699+82_1699+83delinsAC
ENST00000444666.6:c.1699+82_1699+83delinsAC ENSP00000415447.2:n.1699+82_1699+83delinsAC
ENST00000470392.2:n.1789+82_1789+83delinsAC
ENST00000485784.2:n.1778+82_1778+83delinsAC
ENST00000674616.1:c.*1413+82_*1413+83delinsAC ENSP00000502408.1:n.*1413+82_*1413+83delinsAC
ENST00000674643.1:c.*799+82_*799+83delinsAC ENSP00000501636.1:n.*799+82_*799+83delinsAC
ENST00000674737.1:c.*1037+82_*1037+83delinsAC ENSP00000502464.1:n.*1037+82_*1037+83delinsAC
ENST00000674807.1:c.1614-2159_1614-2158delinsAC ENSP00000502814.1:n.1614-2159_1614-2158delinsAC
ENST00000674815.1:c.1330+82_1330+83delinsAC ENSP00000502799.1:n.1330+82_1330+83delinsAC
ENST00000674851.1:c.1330+82_1330+83delinsAC ENSP00000502451.1:n.1330+82_1330+83delinsAC
ENST00000674969.1:n.3572+82_3572+83delinsAC
ENST00000675051.1:c.1498+82_1498+83delinsAC ENSP00000502296.1:n.1498+82_1498+83delinsAC
ENST00000675529.1:c.*1569+82_*1569+83delinsAC ENSP00000501655.1:n.*1569+82_*1569+83delinsAC
ENST00000675587.1:n.2531+82_2531+83delinsAC
ENST00000675651.1:c.1699+82_1699+83delinsAC ENSP00000502513.1:n.1699+82_1699+83delinsAC
ENST00000675693.1:c.1531+82_1531+83delinsAC ENSP00000502174.1:n.1531+82_1531+83delinsAC
ENST00000675810.1:c.1597+82_1597+83delinsAC ENSP00000502743.1:n.1597+82_1597+83delinsAC
ENST00000675859.1:c.1614-2159_1614-2158delinsAC ENSP00000502033.1:n.1614-2159_1614-2158delinsAC
ENST00000675863.1:n.1707+82_1707+83delinsAC
ENST00000675886.1:n.7739+82_7739+83delinsAC
ENST00000676088.1:c.*1641+82_*1641+83delinsAC ENSP00000501884.1:n.*1641+82_*1641+83delinsAC
ENST00000676140.1:c.*644+82_*644+83delinsAC ENSP00000502571.1:n.*644+82_*644+83delinsAC
ENST00000676164.1:c.*1150+82_*1150+83delinsAC ENSP00000501986.1:n.*1150+82_*1150+83delinsAC
ENST00000676210.1:c.*988+82_*988+83delinsAC ENSP00000502373.1:n.*988+82_*988+83delinsAC
ENST00000676259.1:c.*1131+82_*1131+83delinsAC ENSP00000501980.1:n.*1131+82_*1131+83delinsAC
ENST00000676403.1:c.1699+82_1699+83delinsAC ENSP00000502681.1:n.1699+82_1699+83delinsAC
ENST00000389266.7:c.1699+82_1699+83delinsAC ENSP00000373918.3:n.1699+82_1699+83delinsAC
ENST00000444666.5:c.220+82_220+83delinsAC ENSP00000415447.1:n.220+82_220+83delinsAC
ENST00000470392.1:n.421+82_421+83delinsAC
NM_001316772.1:c.1537+82_1537+83delinsAC NP_001303701.1:n.1537+82_1537+83delinsAC
NM_002047.2:c.1699+82_1699+83delinsAC , LRG_243t1:c.1699+82_1699+83delinsAC NP_002038.2:n.1699+82_1699+83delinsAC
NM_002047.3:c.1699+82_1699+83delinsAC NP_002038.2:n.1699+82_1699+83delinsAC
XM_006715686.1:c.1330+82_1330+83delinsAC XP_006715749.1:n.1330+82_1330+83delinsAC
XM_006715686.2:c.1330+82_1330+83delinsAC XP_006715749.1:n.1330+82_1330+83delinsAC
NM_002047.4:c.1699+82_1699+83delinsAC MANE Select NP_002038.2:n.1699+82_1699+83delinsAC