Canonical Allele Identifier: CA1697807403
Gene: GARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30609572A= , CM000669.2:g.30609572A= GRCh38
NC_000007.13:g.30649188A= , CM000669.1:g.30649188A= GRCh37
NC_000007.12:g.30615713A= NCBI36
NG_007942.1:g.20008A= , LRG_243:g.20008A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389266.8:c.736-13A= MANE Select ENSP00000373918.3:n.736-13A=
ENST00000444666.6:c.736-13A= ENSP00000415447.2:n.736-13A=
ENST00000470392.2:n.826-13A=
ENST00000478124.6:n.799-13A=
ENST00000485784.2:n.815-13A=
ENST00000674616.1:c.*450-13A= ENSP00000502408.1:n.*450-13A=
ENST00000674643.1:c.736-13A= ENSP00000501636.1:n.736-13A=
ENST00000674734.1:n.1232-13A=
ENST00000674737.1:c.*74-13A= ENSP00000502464.1:n.*74-13A=
ENST00000674807.1:c.736-13A= ENSP00000502814.1:n.736-13A=
ENST00000674815.1:c.367-13A= ENSP00000502799.1:n.367-13A=
ENST00000674851.1:c.367-13A= ENSP00000502451.1:n.367-13A=
ENST00000674969.1:n.2609-13A=
ENST00000675051.1:c.535-13A= ENSP00000502296.1:n.535-13A=
ENST00000675529.1:c.*606-13A= ENSP00000501655.1:n.*606-13A=
ENST00000675587.1:n.752-13A=
ENST00000675651.1:c.736-13A= ENSP00000502513.1:n.736-13A=
ENST00000675693.1:c.568-13A= ENSP00000502174.1:n.568-13A=
ENST00000675810.1:c.634-13A= ENSP00000502743.1:n.634-13A=
ENST00000675859.1:c.736-13A= ENSP00000502033.1:n.736-13A=
ENST00000675863.1:n.744-13A=
ENST00000675886.1:n.6763A=
ENST00000676088.1:c.*678-13A= ENSP00000501884.1:n.*678-13A=
ENST00000676140.1:c.736-13A= ENSP00000502571.1:n.736-13A=
ENST00000676164.1:c.*187-13A= ENSP00000501986.1:n.*187-13A=
ENST00000676210.1:c.*25-13A= ENSP00000502373.1:n.*25-13A=
ENST00000676259.1:c.*168-13A= ENSP00000501980.1:n.*168-13A=
ENST00000676403.1:c.736-13A= ENSP00000502681.1:n.736-13A=
ENST00000389266.7:c.736-13A= ENSP00000373918.3:n.736-13A=
ENST00000478124.5:n.774-13A=
NM_001316772.1:c.574-13A= NP_001303701.1:n.574-13A=
NM_002047.2:c.736-13A= , LRG_243t1:c.736-13A= NP_002038.2:n.736-13A=
NM_002047.3:c.736-13A= NP_002038.2:n.736-13A=
XM_006715686.1:c.367-13A= XP_006715749.1:n.367-13A=
XM_006715686.2:c.367-13A= XP_006715749.1:n.367-13A=
NM_002047.4:c.736-13A= MANE Select NP_002038.2:n.736-13A=