Canonical Allele Identifier: CA1697769741
Gene: GARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30621498C= , CM000669.2:g.30621498C= GRCh38
NC_000007.13:g.30661114C= , CM000669.1:g.30661114C= GRCh37
NC_000007.12:g.30627639C= NCBI36
NG_007942.1:g.31934C= , LRG_243:g.31934C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389266.8:c.1465C= MANE Select ENSP00000373918.3:p.Pro489=
ENST00000444666.6:c.1465C= ENSP00000415447.2:p.Pro489=
ENST00000470392.2:n.1555C=
ENST00000478124.6:n.1528C=
ENST00000485784.2:n.1544C=
ENST00000674616.1:c.*1179C= ENSP00000502408.1:n.*1179C=
ENST00000674643.1:c.*565C= ENSP00000501636.1:n.*565C=
ENST00000674734.1:n.1961C=
ENST00000674737.1:c.*803C= ENSP00000502464.1:n.*803C=
ENST00000674807.1:c.1465C= ENSP00000502814.1:p.Pro489=
ENST00000674815.1:c.1096C= ENSP00000502799.1:p.Pro366=
ENST00000674851.1:c.1096C= ENSP00000502451.1:p.Pro366=
ENST00000674969.1:n.3338C=
ENST00000675051.1:c.1264C= ENSP00000502296.1:p.Pro422=
ENST00000675529.1:c.*1335C= ENSP00000501655.1:n.*1335C=
ENST00000675587.1:n.1481C=
ENST00000675651.1:c.1465C= ENSP00000502513.1:p.Pro489=
ENST00000675693.1:c.1297C= ENSP00000502174.1:p.Pro433=
ENST00000675810.1:c.1363C= ENSP00000502743.1:p.Pro455=
ENST00000675859.1:c.1465C= ENSP00000502033.1:p.Pro489=
ENST00000675863.1:n.1473C=
ENST00000675886.1:n.7505C=
ENST00000676088.1:c.*1407C= ENSP00000501884.1:n.*1407C=
ENST00000676140.1:c.*410C= ENSP00000502571.1:n.*410C=
ENST00000676164.1:c.*916C= ENSP00000501986.1:n.*916C=
ENST00000676210.1:c.*754C= ENSP00000502373.1:n.*754C=
ENST00000676259.1:c.*897C= ENSP00000501980.1:n.*897C=
ENST00000676403.1:c.1465C= ENSP00000502681.1:p.Pro489=
ENST00000389266.7:c.1465C= ENSP00000373918.3:p.Pro489=
ENST00000478124.5:n.1503C=
ENST00000484093.1:n.464C=
NM_001316772.1:c.1303C= NP_001303701.1:p.Pro435=
NM_002047.2:c.1465C= , LRG_243t1:c.1465C= NP_002038.2:p.Pro489=
NM_002047.3:c.1465C= NP_002038.2:p.Pro489=
XM_006715686.1:c.1096C= XP_006715749.1:p.Pro366=
XM_006715686.2:c.1096C= XP_006715749.1:p.Pro366=
NM_002047.4:c.1465C= MANE Select NP_002038.2:p.Pro489=