Canonical Allele Identifier: CA367125547
Community Standard Title: NM_002047.4(GARS1):c.1007C>G (p.Pro336Arg)
Gene: GARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30612221C>G , CM000669.2:g.30612221C>G GRCh38
NC_000007.13:g.30651837C>G , CM000669.1:g.30651837C>G GRCh37
NC_000007.12:g.30618362C>G NCBI36
NG_007942.1:g.22657C>G , LRG_243:g.22657C>G

Transcript Alleles

HGVS Amino-acid Change
NM_002047.4:c.1007C>G MANE Select NP_002038.2:p.Pro336Arg
ENST00000389266.8:c.1007C>G MANE Select ENSP00000373918.3:p.Pro336Arg
NM_001316772.1:c.845C>G NP_001303701.1:p.Pro282Arg
NM_002047.2:c.1007C>G , LRG_243t1:c.1007C>G NP_002038.2:p.Pro336Arg
NM_002047.3:c.1007C>G NP_002038.2:p.Pro336Arg
ENST00000389266.7:c.1007C>G ENSP00000373918.3:p.Pro336Arg
ENST00000444666.6:c.1007C>G ENSP00000415447.2:p.Pro336Arg
ENST00000470392.2:n.1097C>G
ENST00000478124.5:n.1045C>G
ENST00000478124.6:n.1070C>G
ENST00000485784.2:n.1086C>G
ENST00000674616.1:c.*721C>G ENSP00000502408.1:n.*721C>G
ENST00000674643.1:c.1007C>G ENSP00000501636.1:p.Pro336Arg
ENST00000674734.1:n.1503C>G
ENST00000674737.1:c.*345C>G ENSP00000502464.1:n.*345C>G
ENST00000674807.1:c.1007C>G ENSP00000502814.1:p.Pro336Arg
ENST00000674815.1:c.638C>G ENSP00000502799.1:p.Pro213Arg
ENST00000674851.1:c.638C>G ENSP00000502451.1:p.Pro213Arg
ENST00000674969.1:n.2880C>G
ENST00000675051.1:c.806C>G ENSP00000502296.1:p.Pro269Arg
ENST00000675529.1:c.*877C>G ENSP00000501655.1:n.*877C>G
ENST00000675587.1:n.1023C>G
ENST00000675651.1:c.1007C>G ENSP00000502513.1:p.Pro336Arg
ENST00000675693.1:c.839C>G ENSP00000502174.1:p.Pro280Arg
ENST00000675810.1:c.905C>G ENSP00000502743.1:p.Pro302Arg
ENST00000675859.1:c.1007C>G ENSP00000502033.1:p.Pro336Arg
ENST00000675863.1:n.1015C>G
ENST00000675886.1:n.7047C>G
ENST00000676088.1:c.*949C>G ENSP00000501884.1:n.*949C>G
ENST00000676140.1:c.1007C>G ENSP00000502571.1:p.Pro336Arg
ENST00000676164.1:c.*458C>G ENSP00000501986.1:n.*458C>G
ENST00000676210.1:c.*296C>G ENSP00000502373.1:n.*296C>G
ENST00000676259.1:c.*439C>G ENSP00000501980.1:n.*439C>G
ENST00000676403.1:c.1007C>G ENSP00000502681.1:p.Pro336Arg
XM_006715686.1:c.638C>G XP_006715749.1:p.Pro213Arg
XM_006715686.2:c.638C>G XP_006715749.1:p.Pro213Arg