Canonical Allele Identifier: CA1697807373
Gene: GARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30609548T= , CM000669.2:g.30609548T= GRCh38
NC_000007.13:g.30649164T= , CM000669.1:g.30649164T= GRCh37
NC_000007.12:g.30615689T= NCBI36
NG_007942.1:g.19984T= , LRG_243:g.19984T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389266.8:c.736-37T= MANE Select ENSP00000373918.3:n.736-37T=
ENST00000444666.6:c.736-37T= ENSP00000415447.2:n.736-37T=
ENST00000470392.2:n.826-37T=
ENST00000478124.6:n.799-37T=
ENST00000485784.2:n.815-37T=
ENST00000674616.1:c.*450-37T= ENSP00000502408.1:n.*450-37T=
ENST00000674643.1:c.736-37T= ENSP00000501636.1:n.736-37T=
ENST00000674734.1:n.1232-37T=
ENST00000674737.1:c.*74-37T= ENSP00000502464.1:n.*74-37T=
ENST00000674807.1:c.736-37T= ENSP00000502814.1:n.736-37T=
ENST00000674815.1:c.367-37T= ENSP00000502799.1:n.367-37T=
ENST00000674851.1:c.367-37T= ENSP00000502451.1:n.367-37T=
ENST00000674969.1:n.2609-37T=
ENST00000675051.1:c.535-37T= ENSP00000502296.1:n.535-37T=
ENST00000675529.1:c.*606-37T= ENSP00000501655.1:n.*606-37T=
ENST00000675587.1:n.752-37T=
ENST00000675651.1:c.736-37T= ENSP00000502513.1:n.736-37T=
ENST00000675693.1:c.568-37T= ENSP00000502174.1:n.568-37T=
ENST00000675810.1:c.634-37T= ENSP00000502743.1:n.634-37T=
ENST00000675859.1:c.736-37T= ENSP00000502033.1:n.736-37T=
ENST00000675863.1:n.744-37T=
ENST00000675886.1:n.6739T=
ENST00000676088.1:c.*678-37T= ENSP00000501884.1:n.*678-37T=
ENST00000676140.1:c.736-37T= ENSP00000502571.1:n.736-37T=
ENST00000676164.1:c.*187-37T= ENSP00000501986.1:n.*187-37T=
ENST00000676210.1:c.*25-37T= ENSP00000502373.1:n.*25-37T=
ENST00000676259.1:c.*168-37T= ENSP00000501980.1:n.*168-37T=
ENST00000676403.1:c.736-37T= ENSP00000502681.1:n.736-37T=
ENST00000389266.7:c.736-37T= ENSP00000373918.3:n.736-37T=
ENST00000478124.5:n.774-37T=
NM_001316772.1:c.574-37T= NP_001303701.1:n.574-37T=
NM_002047.2:c.736-37T= , LRG_243t1:c.736-37T= NP_002038.2:n.736-37T=
NM_002047.3:c.736-37T= NP_002038.2:n.736-37T=
XM_006715686.1:c.367-37T= XP_006715749.1:n.367-37T=
XM_006715686.2:c.367-37T= XP_006715749.1:n.367-37T=
NM_002047.4:c.736-37T= MANE Select NP_002038.2:n.736-37T=