Canonical Allele Identifier: CA367124845

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30651723C>G (hg19) ; chr7:g.30612107C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612107C>G , CM000669.2:g.30612107C>G	GRCh38
NC_000007.13:g.30651723C>G , CM000669.1:g.30651723C>G	GRCh37
NC_000007.12:g.30618248C>G	NCBI36
NG_007942.1:g.22543C>G , LRG_243:g.22543C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.893C>G MANE Select	ENSP00000373918.3:p.Pro298Arg
ENST00000444666.6:c.893C>G	ENSP00000415447.2:p.Pro298Arg
ENST00000470392.2:n.983C>G
ENST00000478124.6:n.956C>G
ENST00000485784.2:n.972C>G
ENST00000674616.1:c.*607C>G	ENSP00000502408.1:n.*607C>G
ENST00000674643.1:c.893C>G	ENSP00000501636.1:p.Pro298Arg
ENST00000674734.1:n.1389C>G
ENST00000674737.1:c.*231C>G	ENSP00000502464.1:n.*231C>G
ENST00000674807.1:c.893C>G	ENSP00000502814.1:p.Pro298Arg
ENST00000674815.1:c.524C>G	ENSP00000502799.1:p.Pro175Arg
ENST00000674851.1:c.524C>G	ENSP00000502451.1:p.Pro175Arg
ENST00000674969.1:n.2766C>G
ENST00000675051.1:c.692C>G	ENSP00000502296.1:p.Pro231Arg
ENST00000675529.1:c.*763C>G	ENSP00000501655.1:n.*763C>G
ENST00000675587.1:n.909C>G
ENST00000675651.1:c.893C>G	ENSP00000502513.1:p.Pro298Arg
ENST00000675693.1:c.725C>G	ENSP00000502174.1:p.Pro242Arg
ENST00000675810.1:c.791C>G	ENSP00000502743.1:p.Pro264Arg
ENST00000675859.1:c.893C>G	ENSP00000502033.1:p.Pro298Arg
ENST00000675863.1:n.901C>G
ENST00000675886.1:n.6933C>G
ENST00000676088.1:c.*835C>G	ENSP00000501884.1:n.*835C>G
ENST00000676140.1:c.893C>G	ENSP00000502571.1:p.Pro298Arg
ENST00000676164.1:c.*344C>G	ENSP00000501986.1:n.*344C>G
ENST00000676210.1:c.*182C>G	ENSP00000502373.1:n.*182C>G
ENST00000676259.1:c.*325C>G	ENSP00000501980.1:n.*325C>G
ENST00000676403.1:c.893C>G	ENSP00000502681.1:p.Pro298Arg
ENST00000389266.7:c.893C>G	ENSP00000373918.3:p.Pro298Arg
ENST00000478124.5:n.931C>G
NM_001316772.1:c.731C>G	NP_001303701.1:p.Pro244Arg
NM_002047.2:c.893C>G , LRG_243t1:c.893C>G	NP_002038.2:p.Pro298Arg
NM_002047.3:c.893C>G	NP_002038.2:p.Pro298Arg
XM_006715686.1:c.524C>G	XP_006715749.1:p.Pro175Arg
XM_006715686.2:c.524C>G	XP_006715749.1:p.Pro175Arg
NM_002047.4:c.893C>G MANE Select	NP_002038.2:p.Pro298Arg