Canonical Allele Identifier: CA1697811103
Gene: GARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30612156C= , CM000669.2:g.30612156C= GRCh38
NC_000007.13:g.30651772C= , CM000669.1:g.30651772C= GRCh37
NC_000007.12:g.30618297C= NCBI36
NG_007942.1:g.22592C= , LRG_243:g.22592C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389266.8:c.942C= MANE Select ENSP00000373918.3:p.Phe314=
ENST00000444666.6:c.942C= ENSP00000415447.2:p.Phe314=
ENST00000470392.2:n.1032C=
ENST00000478124.6:n.1005C=
ENST00000485784.2:n.1021C=
ENST00000674616.1:c.*656C= ENSP00000502408.1:n.*656C=
ENST00000674643.1:c.942C= ENSP00000501636.1:p.Phe314=
ENST00000674734.1:n.1438C=
ENST00000674737.1:c.*280C= ENSP00000502464.1:n.*280C=
ENST00000674807.1:c.942C= ENSP00000502814.1:p.Phe314=
ENST00000674815.1:c.573C= ENSP00000502799.1:p.Phe191=
ENST00000674851.1:c.573C= ENSP00000502451.1:p.Phe191=
ENST00000674969.1:n.2815C=
ENST00000675051.1:c.741C= ENSP00000502296.1:p.Phe247=
ENST00000675529.1:c.*812C= ENSP00000501655.1:n.*812C=
ENST00000675587.1:n.958C=
ENST00000675651.1:c.942C= ENSP00000502513.1:p.Phe314=
ENST00000675693.1:c.774C= ENSP00000502174.1:p.Phe258=
ENST00000675810.1:c.840C= ENSP00000502743.1:p.Phe280=
ENST00000675859.1:c.942C= ENSP00000502033.1:p.Phe314=
ENST00000675863.1:n.950C=
ENST00000675886.1:n.6982C=
ENST00000676088.1:c.*884C= ENSP00000501884.1:n.*884C=
ENST00000676140.1:c.942C= ENSP00000502571.1:p.Phe314=
ENST00000676164.1:c.*393C= ENSP00000501986.1:n.*393C=
ENST00000676210.1:c.*231C= ENSP00000502373.1:n.*231C=
ENST00000676259.1:c.*374C= ENSP00000501980.1:n.*374C=
ENST00000676403.1:c.942C= ENSP00000502681.1:p.Phe314=
ENST00000389266.7:c.942C= ENSP00000373918.3:p.Phe314=
ENST00000478124.5:n.980C=
NM_001316772.1:c.780C= NP_001303701.1:p.Phe260=
NM_002047.2:c.942C= , LRG_243t1:c.942C= NP_002038.2:p.Phe314=
NM_002047.3:c.942C= NP_002038.2:p.Phe314=
XM_006715686.1:c.573C= XP_006715749.1:p.Phe191=
XM_006715686.2:c.573C= XP_006715749.1:p.Phe191=
NM_002047.4:c.942C= MANE Select NP_002038.2:p.Phe314=