Canonical Allele Identifier: CA2682252020
Gene: GARS1 HGNC NCBI

Linked Data

gnomAD v4: 7-30631390-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30631390A>G , CM000669.2:g.30631390A>G GRCh38
NC_000007.13:g.30671006A>G , CM000669.1:g.30671006A>G GRCh37
NC_000007.12:g.30637531A>G NCBI36
NG_007942.1:g.41826A>G , LRG_243:g.41826A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000389266.8:c.1810-58A>G MANE Select ENSP00000373918.3:n.1810-58A>G
ENST00000444666.6:c.*231-58A>G ENSP00000415447.2:n.*231-58A>G
ENST00000465748.2:n.1291-58A>G
ENST00000470392.2:n.4620A>G
ENST00000485784.2:n.4609A>G
ENST00000496643.2:n.2847A>G
ENST00000674616.1:c.*1524-58A>G ENSP00000502408.1:n.*1524-58A>G
ENST00000674643.1:c.*910-58A>G ENSP00000501636.1:n.*910-58A>G
ENST00000674737.1:c.*1148-58A>G ENSP00000502464.1:n.*1148-58A>G
ENST00000674807.1:c.*83-58A>G ENSP00000502814.1:n.*83-58A>G
ENST00000674815.1:c.1441-58A>G ENSP00000502799.1:n.1441-58A>G
ENST00000674851.1:c.1441-58A>G ENSP00000502451.1:n.1441-58A>G
ENST00000674969.1:n.3683-58A>G
ENST00000675051.1:c.1609-58A>G ENSP00000502296.1:n.1609-58A>G
ENST00000675529.1:c.*1680-58A>G ENSP00000501655.1:n.*1680-58A>G
ENST00000675587.1:n.2642-58A>G
ENST00000675651.1:c.1810-58A>G ENSP00000502513.1:n.1810-58A>G
ENST00000675693.1:c.1642-58A>G ENSP00000502174.1:n.1642-58A>G
ENST00000675810.1:c.1708-58A>G ENSP00000502743.1:n.1708-58A>G
ENST00000675859.1:c.*83-857A>G ENSP00000502033.1:n.*83-857A>G
ENST00000675863.1:n.1818-58A>G
ENST00000675886.1:n.7850-58A>G
ENST00000676088.1:c.*1752-58A>G ENSP00000501884.1:n.*1752-58A>G
ENST00000676140.1:c.*755-58A>G ENSP00000502571.1:n.*755-58A>G
ENST00000676164.1:c.*1261-58A>G ENSP00000501986.1:n.*1261-58A>G
ENST00000676210.1:c.*1099-58A>G ENSP00000502373.1:n.*1099-58A>G
ENST00000676259.1:c.*1242-58A>G ENSP00000501980.1:n.*1242-58A>G
ENST00000676403.1:c.1810-857A>G ENSP00000502681.1:n.1810-857A>G
ENST00000389266.7:c.1810-58A>G ENSP00000373918.3:n.1810-58A>G
ENST00000444666.5:c.465-58A>G ENSP00000415447.1:n.465-58A>G
ENST00000465748.1:n.181-58A>G
ENST00000485784.1:n.242A>G
NM_001316772.1:c.1648-58A>G NP_001303701.1:n.1648-58A>G
NM_002047.2:c.1810-58A>G , LRG_243t1:c.1810-58A>G NP_002038.2:n.1810-58A>G
NM_002047.3:c.1810-58A>G NP_002038.2:n.1810-58A>G
XM_006715686.1:c.1441-58A>G XP_006715749.1:n.1441-58A>G
XM_006715686.2:c.1441-58A>G XP_006715749.1:n.1441-58A>G
NM_002047.4:c.1810-58A>G MANE Select NP_002038.2:n.1810-58A>G