Canonical Allele Identifier: CA367124368

Gene: GARS1

Linked Data

• gnomAD v4: 7-30609646-C-G
• MyVariant Identifiers: chr7:g.30649262C>G (hg19) ; chr7:g.30609646C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30609646C>G , CM000669.2:g.30609646C>G	GRCh38
NC_000007.13:g.30649262C>G , CM000669.1:g.30649262C>G	GRCh37
NC_000007.12:g.30615787C>G	NCBI36
NG_007942.1:g.20082C>G , LRG_243:g.20082C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.797C>G MANE Select	ENSP00000373918.3:p.Pro266Arg
ENST00000444666.6:c.797C>G	ENSP00000415447.2:p.Pro266Arg
ENST00000470392.2:n.887C>G
ENST00000478124.6:n.860C>G
ENST00000485784.2:n.876C>G
ENST00000674616.1:c.*511C>G	ENSP00000502408.1:n.*511C>G
ENST00000674643.1:c.797C>G	ENSP00000501636.1:p.Pro266Arg
ENST00000674734.1:n.1293C>G
ENST00000674737.1:c.*135C>G	ENSP00000502464.1:n.*135C>G
ENST00000674807.1:c.797C>G	ENSP00000502814.1:p.Pro266Arg
ENST00000674815.1:c.428C>G	ENSP00000502799.1:p.Pro143Arg
ENST00000674851.1:c.428C>G	ENSP00000502451.1:p.Pro143Arg
ENST00000674969.1:n.2670C>G
ENST00000675051.1:c.596C>G	ENSP00000502296.1:p.Pro199Arg
ENST00000675529.1:c.*667C>G	ENSP00000501655.1:n.*667C>G
ENST00000675587.1:n.813C>G
ENST00000675651.1:c.797C>G	ENSP00000502513.1:p.Pro266Arg
ENST00000675693.1:c.629C>G	ENSP00000502174.1:p.Pro210Arg
ENST00000675810.1:c.695C>G	ENSP00000502743.1:p.Pro232Arg
ENST00000675859.1:c.797C>G	ENSP00000502033.1:p.Pro266Arg
ENST00000675863.1:n.805C>G
ENST00000675886.1:n.6837C>G
ENST00000676088.1:c.*739C>G	ENSP00000501884.1:n.*739C>G
ENST00000676140.1:c.797C>G	ENSP00000502571.1:p.Pro266Arg
ENST00000676164.1:c.*248C>G	ENSP00000501986.1:n.*248C>G
ENST00000676210.1:c.*86C>G	ENSP00000502373.1:n.*86C>G
ENST00000676259.1:c.*229C>G	ENSP00000501980.1:n.*229C>G
ENST00000676403.1:c.797C>G	ENSP00000502681.1:p.Pro266Arg
ENST00000389266.7:c.797C>G	ENSP00000373918.3:p.Pro266Arg
ENST00000478124.5:n.835C>G
NM_001316772.1:c.635C>G	NP_001303701.1:p.Pro212Arg
NM_002047.2:c.797C>G , LRG_243t1:c.797C>G	NP_002038.2:p.Pro266Arg
NM_002047.3:c.797C>G	NP_002038.2:p.Pro266Arg
XM_006715686.1:c.428C>G	XP_006715749.1:p.Pro143Arg
XM_006715686.2:c.428C>G	XP_006715749.1:p.Pro143Arg
NM_002047.4:c.797C>G MANE Select	NP_002038.2:p.Pro266Arg