Canonical Allele Identifier: CA1697810857
Gene: GARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30612002A= , CM000669.2:g.30612002A= GRCh38
NC_000007.13:g.30651618A= , CM000669.1:g.30651618A= GRCh37
NC_000007.12:g.30618143A= NCBI36
NG_007942.1:g.22438A= , LRG_243:g.22438A=

Transcript Alleles

HGVS Amino-acid change
ENST00000389266.8:c.882-94A= MANE Select ENSP00000373918.3:n.882-94A=
ENST00000444666.6:c.882-94A= ENSP00000415447.2:n.882-94A=
ENST00000470392.2:n.972-94A=
ENST00000478124.6:n.945-94A=
ENST00000485784.2:n.961-94A=
ENST00000674616.1:c.*596-94A= ENSP00000502408.1:n.*596-94A=
ENST00000674643.1:c.882-94A= ENSP00000501636.1:n.882-94A=
ENST00000674734.1:n.1378-94A=
ENST00000674737.1:c.*220-94A= ENSP00000502464.1:n.*220-94A=
ENST00000674807.1:c.882-94A= ENSP00000502814.1:n.882-94A=
ENST00000674815.1:c.513-94A= ENSP00000502799.1:n.513-94A=
ENST00000674851.1:c.513-94A= ENSP00000502451.1:n.513-94A=
ENST00000674969.1:n.2755-94A=
ENST00000675051.1:c.681-94A= ENSP00000502296.1:n.681-94A=
ENST00000675529.1:c.*752-94A= ENSP00000501655.1:n.*752-94A=
ENST00000675587.1:n.898-94A=
ENST00000675651.1:c.882-94A= ENSP00000502513.1:n.882-94A=
ENST00000675693.1:c.714-94A= ENSP00000502174.1:n.714-94A=
ENST00000675810.1:c.780-94A= ENSP00000502743.1:n.780-94A=
ENST00000675859.1:c.882-94A= ENSP00000502033.1:n.882-94A=
ENST00000675863.1:n.890-94A=
ENST00000675886.1:n.6922-94A=
ENST00000676088.1:c.*824-94A= ENSP00000501884.1:n.*824-94A=
ENST00000676140.1:c.882-94A= ENSP00000502571.1:n.882-94A=
ENST00000676164.1:c.*333-94A= ENSP00000501986.1:n.*333-94A=
ENST00000676210.1:c.*171-94A= ENSP00000502373.1:n.*171-94A=
ENST00000676259.1:c.*314-94A= ENSP00000501980.1:n.*314-94A=
ENST00000676403.1:c.882-94A= ENSP00000502681.1:n.882-94A=
ENST00000389266.7:c.882-94A= ENSP00000373918.3:n.882-94A=
ENST00000478124.5:n.920-94A=
NM_001316772.1:c.720-94A= NP_001303701.1:n.720-94A=
NM_002047.2:c.882-94A= , LRG_243t1:c.882-94A= NP_002038.2:n.882-94A=
NM_002047.3:c.882-94A= NP_002038.2:n.882-94A=
XM_006715686.1:c.513-94A= XP_006715749.1:n.513-94A=
XM_006715686.2:c.513-94A= XP_006715749.1:n.513-94A=
NM_002047.4:c.882-94A= MANE Select NP_002038.2:n.882-94A=