Canonical Allele Identifier: CA367125060
Gene: GARS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.30612166A>T , CM000669.2:g.30612166A>T GRCh38
NC_000007.13:g.30651782A>T , CM000669.1:g.30651782A>T GRCh37
NC_000007.12:g.30618307A>T NCBI36
NG_007942.1:g.22602A>T , LRG_243:g.22602A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000389266.8:c.952A>T MANE Select ENSP00000373918.3:p.Lys318Ter
ENST00000444666.6:c.952A>T ENSP00000415447.2:p.Lys318Ter
ENST00000470392.2:n.1042A>T
ENST00000478124.6:n.1015A>T
ENST00000485784.2:n.1031A>T
ENST00000674616.1:c.*666A>T ENSP00000502408.1:n.*666A>T
ENST00000674643.1:c.952A>T ENSP00000501636.1:p.Lys318Ter
ENST00000674734.1:n.1448A>T
ENST00000674737.1:c.*290A>T ENSP00000502464.1:n.*290A>T
ENST00000674807.1:c.952A>T ENSP00000502814.1:p.Lys318Ter
ENST00000674815.1:c.583A>T ENSP00000502799.1:p.Lys195Ter
ENST00000674851.1:c.583A>T ENSP00000502451.1:p.Lys195Ter
ENST00000674969.1:n.2825A>T
ENST00000675051.1:c.751A>T ENSP00000502296.1:p.Lys251Ter
ENST00000675529.1:c.*822A>T ENSP00000501655.1:n.*822A>T
ENST00000675587.1:n.968A>T
ENST00000675651.1:c.952A>T ENSP00000502513.1:p.Lys318Ter
ENST00000675693.1:c.784A>T ENSP00000502174.1:p.Lys262Ter
ENST00000675810.1:c.850A>T ENSP00000502743.1:p.Lys284Ter
ENST00000675859.1:c.952A>T ENSP00000502033.1:p.Lys318Ter
ENST00000675863.1:n.960A>T
ENST00000675886.1:n.6992A>T
ENST00000676088.1:c.*894A>T ENSP00000501884.1:n.*894A>T
ENST00000676140.1:c.952A>T ENSP00000502571.1:p.Lys318Ter
ENST00000676164.1:c.*403A>T ENSP00000501986.1:n.*403A>T
ENST00000676210.1:c.*241A>T ENSP00000502373.1:n.*241A>T
ENST00000676259.1:c.*384A>T ENSP00000501980.1:n.*384A>T
ENST00000676403.1:c.952A>T ENSP00000502681.1:p.Lys318Ter
ENST00000389266.7:c.952A>T ENSP00000373918.3:p.Lys318Ter
ENST00000478124.5:n.990A>T
NM_001316772.1:c.790A>T NP_001303701.1:p.Lys264Ter
NM_002047.2:c.952A>T , LRG_243t1:c.952A>T NP_002038.2:p.Lys318Ter
NM_002047.3:c.952A>T NP_002038.2:p.Lys318Ter
XM_006715686.1:c.583A>T XP_006715749.1:p.Lys195Ter
XM_006715686.2:c.583A>T XP_006715749.1:p.Lys195Ter
NM_002047.4:c.952A>T MANE Select NP_002038.2:p.Lys318Ter