Canonical Allele Identifier: CA367124643

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30649321A>G (hg19) ; chr7:g.30609705A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30609705A>G , CM000669.2:g.30609705A>G	GRCh38
NC_000007.13:g.30649321A>G , CM000669.1:g.30649321A>G	GRCh37
NC_000007.12:g.30615846A>G	NCBI36
NG_007942.1:g.20141A>G , LRG_243:g.20141A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.856A>G MANE Select	ENSP00000373918.3:p.Ile286Val
ENST00000444666.6:c.856A>G	ENSP00000415447.2:p.Ile286Val
ENST00000470392.2:n.946A>G
ENST00000478124.6:n.919A>G
ENST00000485784.2:n.935A>G
ENST00000674616.1:c.*570A>G	ENSP00000502408.1:n.*570A>G
ENST00000674643.1:c.856A>G	ENSP00000501636.1:p.Ile286Val
ENST00000674734.1:n.1352A>G
ENST00000674737.1:c.*194A>G	ENSP00000502464.1:n.*194A>G
ENST00000674807.1:c.856A>G	ENSP00000502814.1:p.Ile286Val
ENST00000674815.1:c.487A>G	ENSP00000502799.1:p.Ile163Val
ENST00000674851.1:c.487A>G	ENSP00000502451.1:p.Ile163Val
ENST00000674969.1:n.2729A>G
ENST00000675051.1:c.655A>G	ENSP00000502296.1:p.Ile219Val
ENST00000675529.1:c.*726A>G	ENSP00000501655.1:n.*726A>G
ENST00000675587.1:n.872A>G
ENST00000675651.1:c.856A>G	ENSP00000502513.1:p.Ile286Val
ENST00000675693.1:c.688A>G	ENSP00000502174.1:p.Ile230Val
ENST00000675810.1:c.754A>G	ENSP00000502743.1:p.Ile252Val
ENST00000675859.1:c.856A>G	ENSP00000502033.1:p.Ile286Val
ENST00000675863.1:n.864A>G
ENST00000675886.1:n.6896A>G
ENST00000676088.1:c.*798A>G	ENSP00000501884.1:n.*798A>G
ENST00000676140.1:c.856A>G	ENSP00000502571.1:p.Ile286Val
ENST00000676164.1:c.*307A>G	ENSP00000501986.1:n.*307A>G
ENST00000676210.1:c.*145A>G	ENSP00000502373.1:n.*145A>G
ENST00000676259.1:c.*288A>G	ENSP00000501980.1:n.*288A>G
ENST00000676403.1:c.856A>G	ENSP00000502681.1:p.Ile286Val
ENST00000389266.7:c.856A>G	ENSP00000373918.3:p.Ile286Val
ENST00000478124.5:n.894A>G
NM_001316772.1:c.694A>G	NP_001303701.1:p.Ile232Val
NM_002047.2:c.856A>G , LRG_243t1:c.856A>G	NP_002038.2:p.Ile286Val
NM_002047.3:c.856A>G	NP_002038.2:p.Ile286Val
XM_006715686.1:c.487A>G	XP_006715749.1:p.Ile163Val
XM_006715686.2:c.487A>G	XP_006715749.1:p.Ile163Val
NM_002047.4:c.856A>G MANE Select	NP_002038.2:p.Ile286Val