Canonical Allele Identifier: CA1697807504
Gene: GARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30609613C= , CM000669.2:g.30609613C= GRCh38
NC_000007.13:g.30649229C= , CM000669.1:g.30649229C= GRCh37
NC_000007.12:g.30615754C= NCBI36
NG_007942.1:g.20049C= , LRG_243:g.20049C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389266.8:c.764C= MANE Select ENSP00000373918.3:p.Ala255=
ENST00000444666.6:c.764C= ENSP00000415447.2:p.Ala255=
ENST00000470392.2:n.854C=
ENST00000478124.6:n.827C=
ENST00000485784.2:n.843C=
ENST00000674616.1:c.*478C= ENSP00000502408.1:n.*478C=
ENST00000674643.1:c.764C= ENSP00000501636.1:p.Ala255=
ENST00000674734.1:n.1260C=
ENST00000674737.1:c.*102C= ENSP00000502464.1:n.*102C=
ENST00000674807.1:c.764C= ENSP00000502814.1:p.Ala255=
ENST00000674815.1:c.395C= ENSP00000502799.1:p.Ala132=
ENST00000674851.1:c.395C= ENSP00000502451.1:p.Ala132=
ENST00000674969.1:n.2637C=
ENST00000675051.1:c.563C= ENSP00000502296.1:p.Ala188=
ENST00000675529.1:c.*634C= ENSP00000501655.1:n.*634C=
ENST00000675587.1:n.780C=
ENST00000675651.1:c.764C= ENSP00000502513.1:p.Ala255=
ENST00000675693.1:c.596C= ENSP00000502174.1:p.Ala199=
ENST00000675810.1:c.662C= ENSP00000502743.1:p.Ala221=
ENST00000675859.1:c.764C= ENSP00000502033.1:p.Ala255=
ENST00000675863.1:n.772C=
ENST00000675886.1:n.6804C=
ENST00000676088.1:c.*706C= ENSP00000501884.1:n.*706C=
ENST00000676140.1:c.764C= ENSP00000502571.1:p.Ala255=
ENST00000676164.1:c.*215C= ENSP00000501986.1:n.*215C=
ENST00000676210.1:c.*53C= ENSP00000502373.1:n.*53C=
ENST00000676259.1:c.*196C= ENSP00000501980.1:n.*196C=
ENST00000676403.1:c.764C= ENSP00000502681.1:p.Ala255=
ENST00000389266.7:c.764C= ENSP00000373918.3:p.Ala255=
ENST00000478124.5:n.802C=
NM_001316772.1:c.602C= NP_001303701.1:p.Ala201=
NM_002047.2:c.764C= , LRG_243t1:c.764C= NP_002038.2:p.Ala255=
NM_002047.3:c.764C= NP_002038.2:p.Ala255=
XM_006715686.1:c.395C= XP_006715749.1:p.Ala132=
XM_006715686.2:c.395C= XP_006715749.1:p.Ala132=
NM_002047.4:c.764C= MANE Select NP_002038.2:p.Ala255=