Canonical Allele Identifier: CA367124622

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30649316C>G (hg19) ; chr7:g.30609700C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30609700C>G , CM000669.2:g.30609700C>G	GRCh38
NC_000007.13:g.30649316C>G , CM000669.1:g.30649316C>G	GRCh37
NC_000007.12:g.30615841C>G	NCBI36
NG_007942.1:g.20136C>G , LRG_243:g.20136C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.851C>G MANE Select	ENSP00000373918.3:p.Thr284Ser
ENST00000444666.6:c.851C>G	ENSP00000415447.2:p.Thr284Ser
ENST00000470392.2:n.941C>G
ENST00000478124.6:n.914C>G
ENST00000485784.2:n.930C>G
ENST00000674616.1:c.*565C>G	ENSP00000502408.1:n.*565C>G
ENST00000674643.1:c.851C>G	ENSP00000501636.1:p.Thr284Ser
ENST00000674734.1:n.1347C>G
ENST00000674737.1:c.*189C>G	ENSP00000502464.1:n.*189C>G
ENST00000674807.1:c.851C>G	ENSP00000502814.1:p.Thr284Ser
ENST00000674815.1:c.482C>G	ENSP00000502799.1:p.Thr161Ser
ENST00000674851.1:c.482C>G	ENSP00000502451.1:p.Thr161Ser
ENST00000674969.1:n.2724C>G
ENST00000675051.1:c.650C>G	ENSP00000502296.1:p.Thr217Ser
ENST00000675529.1:c.*721C>G	ENSP00000501655.1:n.*721C>G
ENST00000675587.1:n.867C>G
ENST00000675651.1:c.851C>G	ENSP00000502513.1:p.Thr284Ser
ENST00000675693.1:c.683C>G	ENSP00000502174.1:p.Thr228Ser
ENST00000675810.1:c.749C>G	ENSP00000502743.1:p.Thr250Ser
ENST00000675859.1:c.851C>G	ENSP00000502033.1:p.Thr284Ser
ENST00000675863.1:n.859C>G
ENST00000675886.1:n.6891C>G
ENST00000676088.1:c.*793C>G	ENSP00000501884.1:n.*793C>G
ENST00000676140.1:c.851C>G	ENSP00000502571.1:p.Thr284Ser
ENST00000676164.1:c.*302C>G	ENSP00000501986.1:n.*302C>G
ENST00000676210.1:c.*140C>G	ENSP00000502373.1:n.*140C>G
ENST00000676259.1:c.*283C>G	ENSP00000501980.1:n.*283C>G
ENST00000676403.1:c.851C>G	ENSP00000502681.1:p.Thr284Ser
ENST00000389266.7:c.851C>G	ENSP00000373918.3:p.Thr284Ser
ENST00000478124.5:n.889C>G
NM_001316772.1:c.689C>G	NP_001303701.1:p.Thr230Ser
NM_002047.2:c.851C>G , LRG_243t1:c.851C>G	NP_002038.2:p.Thr284Ser
NM_002047.3:c.851C>G	NP_002038.2:p.Thr284Ser
XM_006715686.1:c.482C>G	XP_006715749.1:p.Thr161Ser
XM_006715686.2:c.482C>G	XP_006715749.1:p.Thr161Ser
NM_002047.4:c.851C>G MANE Select	NP_002038.2:p.Thr284Ser