Canonical Allele Identifier: CA367124863

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30651729C>G (hg19) ; chr7:g.30612113C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612113C>G , CM000669.2:g.30612113C>G	GRCh38
NC_000007.13:g.30651729C>G , CM000669.1:g.30651729C>G	GRCh37
NC_000007.12:g.30618254C>G	NCBI36
NG_007942.1:g.22549C>G , LRG_243:g.22549C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.899C>G MANE Select	ENSP00000373918.3:p.Thr300Ser
ENST00000444666.6:c.899C>G	ENSP00000415447.2:p.Thr300Ser
ENST00000470392.2:n.989C>G
ENST00000478124.6:n.962C>G
ENST00000485784.2:n.978C>G
ENST00000674616.1:c.*613C>G	ENSP00000502408.1:n.*613C>G
ENST00000674643.1:c.899C>G	ENSP00000501636.1:p.Thr300Ser
ENST00000674734.1:n.1395C>G
ENST00000674737.1:c.*237C>G	ENSP00000502464.1:n.*237C>G
ENST00000674807.1:c.899C>G	ENSP00000502814.1:p.Thr300Ser
ENST00000674815.1:c.530C>G	ENSP00000502799.1:p.Thr177Ser
ENST00000674851.1:c.530C>G	ENSP00000502451.1:p.Thr177Ser
ENST00000674969.1:n.2772C>G
ENST00000675051.1:c.698C>G	ENSP00000502296.1:p.Thr233Ser
ENST00000675529.1:c.*769C>G	ENSP00000501655.1:n.*769C>G
ENST00000675587.1:n.915C>G
ENST00000675651.1:c.899C>G	ENSP00000502513.1:p.Thr300Ser
ENST00000675693.1:c.731C>G	ENSP00000502174.1:p.Thr244Ser
ENST00000675810.1:c.797C>G	ENSP00000502743.1:p.Thr266Ser
ENST00000675859.1:c.899C>G	ENSP00000502033.1:p.Thr300Ser
ENST00000675863.1:n.907C>G
ENST00000675886.1:n.6939C>G
ENST00000676088.1:c.*841C>G	ENSP00000501884.1:n.*841C>G
ENST00000676140.1:c.899C>G	ENSP00000502571.1:p.Thr300Ser
ENST00000676164.1:c.*350C>G	ENSP00000501986.1:n.*350C>G
ENST00000676210.1:c.*188C>G	ENSP00000502373.1:n.*188C>G
ENST00000676259.1:c.*331C>G	ENSP00000501980.1:n.*331C>G
ENST00000676403.1:c.899C>G	ENSP00000502681.1:p.Thr300Ser
ENST00000389266.7:c.899C>G	ENSP00000373918.3:p.Thr300Ser
ENST00000478124.5:n.937C>G
NM_001316772.1:c.737C>G	NP_001303701.1:p.Thr246Ser
NM_002047.2:c.899C>G , LRG_243t1:c.899C>G	NP_002038.2:p.Thr300Ser
NM_002047.3:c.899C>G	NP_002038.2:p.Thr300Ser
XM_006715686.1:c.530C>G	XP_006715749.1:p.Thr177Ser
XM_006715686.2:c.530C>G	XP_006715749.1:p.Thr177Ser
NM_002047.4:c.899C>G MANE Select	NP_002038.2:p.Thr300Ser