Canonical Allele Identifier: CA367124572

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30649306A>G (hg19) ; chr7:g.30609690A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30609690A>G , CM000669.2:g.30609690A>G	GRCh38
NC_000007.13:g.30649306A>G , CM000669.1:g.30649306A>G	GRCh37
NC_000007.12:g.30615831A>G	NCBI36
NG_007942.1:g.20126A>G , LRG_243:g.20126A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.841A>G MANE Select	ENSP00000373918.3:p.Met281Val
ENST00000444666.6:c.841A>G	ENSP00000415447.2:p.Met281Val
ENST00000470392.2:n.931A>G
ENST00000478124.6:n.904A>G
ENST00000485784.2:n.920A>G
ENST00000674616.1:c.*555A>G	ENSP00000502408.1:n.*555A>G
ENST00000674643.1:c.841A>G	ENSP00000501636.1:p.Met281Val
ENST00000674734.1:n.1337A>G
ENST00000674737.1:c.*179A>G	ENSP00000502464.1:n.*179A>G
ENST00000674807.1:c.841A>G	ENSP00000502814.1:p.Met281Val
ENST00000674815.1:c.472A>G	ENSP00000502799.1:p.Met158Val
ENST00000674851.1:c.472A>G	ENSP00000502451.1:p.Met158Val
ENST00000674969.1:n.2714A>G
ENST00000675051.1:c.640A>G	ENSP00000502296.1:p.Met214Val
ENST00000675529.1:c.*711A>G	ENSP00000501655.1:n.*711A>G
ENST00000675587.1:n.857A>G
ENST00000675651.1:c.841A>G	ENSP00000502513.1:p.Met281Val
ENST00000675693.1:c.673A>G	ENSP00000502174.1:p.Met225Val
ENST00000675810.1:c.739A>G	ENSP00000502743.1:p.Met247Val
ENST00000675859.1:c.841A>G	ENSP00000502033.1:p.Met281Val
ENST00000675863.1:n.849A>G
ENST00000675886.1:n.6881A>G
ENST00000676088.1:c.*783A>G	ENSP00000501884.1:n.*783A>G
ENST00000676140.1:c.841A>G	ENSP00000502571.1:p.Met281Val
ENST00000676164.1:c.*292A>G	ENSP00000501986.1:n.*292A>G
ENST00000676210.1:c.*130A>G	ENSP00000502373.1:n.*130A>G
ENST00000676259.1:c.*273A>G	ENSP00000501980.1:n.*273A>G
ENST00000676403.1:c.841A>G	ENSP00000502681.1:p.Met281Val
ENST00000389266.7:c.841A>G	ENSP00000373918.3:p.Met281Val
ENST00000478124.5:n.879A>G
NM_001316772.1:c.679A>G	NP_001303701.1:p.Met227Val
NM_002047.2:c.841A>G , LRG_243t1:c.841A>G	NP_002038.2:p.Met281Val
NM_002047.3:c.841A>G	NP_002038.2:p.Met281Val
XM_006715686.1:c.472A>G	XP_006715749.1:p.Met158Val
XM_006715686.2:c.472A>G	XP_006715749.1:p.Met158Val
NM_002047.4:c.841A>G MANE Select	NP_002038.2:p.Met281Val