Canonical Allele Identifier: CA1697769416
Gene: GARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30621343_30621344delinsAT , CM000669.2:g.30621343_30621344delinsAT GRCh38
NC_000007.13:g.30660959_30660960delinsAT , CM000669.1:g.30660959_30660960delinsAT GRCh37
NC_000007.12:g.30627484_30627485delinsAT NCBI36
NG_007942.1:g.31779_31780delinsAT , LRG_243:g.31779_31780delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000389266.8:c.1360-50_1360-49delinsAT MANE Select ENSP00000373918.3:n.1360-50_1360-49delinsAT
ENST00000444666.6:c.1360-50_1360-49delinsAT ENSP00000415447.2:n.1360-50_1360-49delinsAT
ENST00000470392.2:n.1450-50_1450-49delinsAT
ENST00000478124.6:n.1423-50_1423-49delinsAT
ENST00000485784.2:n.1439-50_1439-49delinsAT
ENST00000674616.1:c.*1074-50_*1074-49delinsAT ENSP00000502408.1:n.*1074-50_*1074-49delinsAT
ENST00000674643.1:c.*460-50_*460-49delinsAT ENSP00000501636.1:n.*460-50_*460-49delinsAT
ENST00000674734.1:n.1856-50_1856-49delinsAT
ENST00000674737.1:c.*698-50_*698-49delinsAT ENSP00000502464.1:n.*698-50_*698-49delinsAT
ENST00000674807.1:c.1360-50_1360-49delinsAT ENSP00000502814.1:n.1360-50_1360-49delinsAT
ENST00000674815.1:c.991-50_991-49delinsAT ENSP00000502799.1:n.991-50_991-49delinsAT
ENST00000674851.1:c.991-50_991-49delinsAT ENSP00000502451.1:n.991-50_991-49delinsAT
ENST00000674969.1:n.3233-50_3233-49delinsAT
ENST00000675051.1:c.1159-50_1159-49delinsAT ENSP00000502296.1:n.1159-50_1159-49delinsAT
ENST00000675529.1:c.*1230-50_*1230-49delinsAT ENSP00000501655.1:n.*1230-50_*1230-49delinsAT
ENST00000675587.1:n.1376-50_1376-49delinsAT
ENST00000675651.1:c.1360-50_1360-49delinsAT ENSP00000502513.1:n.1360-50_1360-49delinsAT
ENST00000675693.1:c.1192-50_1192-49delinsAT ENSP00000502174.1:n.1192-50_1192-49delinsAT
ENST00000675810.1:c.1258-50_1258-49delinsAT ENSP00000502743.1:n.1258-50_1258-49delinsAT
ENST00000675859.1:c.1360-50_1360-49delinsAT ENSP00000502033.1:n.1360-50_1360-49delinsAT
ENST00000675863.1:n.1368-50_1368-49delinsAT
ENST00000675886.1:n.7400-50_7400-49delinsAT
ENST00000676088.1:c.*1302-50_*1302-49delinsAT ENSP00000501884.1:n.*1302-50_*1302-49delinsAT
ENST00000676140.1:c.*305-50_*305-49delinsAT ENSP00000502571.1:n.*305-50_*305-49delinsAT
ENST00000676164.1:c.*811-50_*811-49delinsAT ENSP00000501986.1:n.*811-50_*811-49delinsAT
ENST00000676210.1:c.*649-50_*649-49delinsAT ENSP00000502373.1:n.*649-50_*649-49delinsAT
ENST00000676259.1:c.*792-50_*792-49delinsAT ENSP00000501980.1:n.*792-50_*792-49delinsAT
ENST00000676403.1:c.1360-50_1360-49delinsAT ENSP00000502681.1:n.1360-50_1360-49delinsAT
ENST00000389266.7:c.1360-50_1360-49delinsAT ENSP00000373918.3:n.1360-50_1360-49delinsAT
ENST00000478124.5:n.1398-50_1398-49delinsAT
ENST00000484093.1:n.359-50_359-49delinsAT
NM_001316772.1:c.1198-50_1198-49delinsAT NP_001303701.1:n.1198-50_1198-49delinsAT
NM_002047.2:c.1360-50_1360-49delinsAT , LRG_243t1:c.1360-50_1360-49delinsAT NP_002038.2:n.1360-50_1360-49delinsAT
NM_002047.3:c.1360-50_1360-49delinsAT NP_002038.2:n.1360-50_1360-49delinsAT
XM_006715686.1:c.991-50_991-49delinsAT XP_006715749.1:n.991-50_991-49delinsAT
XM_006715686.2:c.991-50_991-49delinsAT XP_006715749.1:n.991-50_991-49delinsAT
NM_002047.4:c.1360-50_1360-49delinsAT MANE Select NP_002038.2:n.1360-50_1360-49delinsAT