Canonical Allele Identifier: CA367124532

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30649298T>G (hg19) ; chr7:g.30609682T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30609682T>G , CM000669.2:g.30609682T>G	GRCh38
NC_000007.13:g.30649298T>G , CM000669.1:g.30649298T>G	GRCh37
NC_000007.12:g.30615823T>G	NCBI36
NG_007942.1:g.20118T>G , LRG_243:g.20118T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.833T>G MANE Select	ENSP00000373918.3:p.Phe278Cys
ENST00000444666.6:c.833T>G	ENSP00000415447.2:p.Phe278Cys
ENST00000470392.2:n.923T>G
ENST00000478124.6:n.896T>G
ENST00000485784.2:n.912T>G
ENST00000674616.1:c.*547T>G	ENSP00000502408.1:n.*547T>G
ENST00000674643.1:c.833T>G	ENSP00000501636.1:p.Phe278Cys
ENST00000674734.1:n.1329T>G
ENST00000674737.1:c.*171T>G	ENSP00000502464.1:n.*171T>G
ENST00000674807.1:c.833T>G	ENSP00000502814.1:p.Phe278Cys
ENST00000674815.1:c.464T>G	ENSP00000502799.1:p.Phe155Cys
ENST00000674851.1:c.464T>G	ENSP00000502451.1:p.Phe155Cys
ENST00000674969.1:n.2706T>G
ENST00000675051.1:c.632T>G	ENSP00000502296.1:p.Phe211Cys
ENST00000675529.1:c.*703T>G	ENSP00000501655.1:n.*703T>G
ENST00000675587.1:n.849T>G
ENST00000675651.1:c.833T>G	ENSP00000502513.1:p.Phe278Cys
ENST00000675693.1:c.665T>G	ENSP00000502174.1:p.Phe222Cys
ENST00000675810.1:c.731T>G	ENSP00000502743.1:p.Phe244Cys
ENST00000675859.1:c.833T>G	ENSP00000502033.1:p.Phe278Cys
ENST00000675863.1:n.841T>G
ENST00000675886.1:n.6873T>G
ENST00000676088.1:c.*775T>G	ENSP00000501884.1:n.*775T>G
ENST00000676140.1:c.833T>G	ENSP00000502571.1:p.Phe278Cys
ENST00000676164.1:c.*284T>G	ENSP00000501986.1:n.*284T>G
ENST00000676210.1:c.*122T>G	ENSP00000502373.1:n.*122T>G
ENST00000676259.1:c.*265T>G	ENSP00000501980.1:n.*265T>G
ENST00000676403.1:c.833T>G	ENSP00000502681.1:p.Phe278Cys
ENST00000389266.7:c.833T>G	ENSP00000373918.3:p.Phe278Cys
ENST00000478124.5:n.871T>G
NM_001316772.1:c.671T>G	NP_001303701.1:p.Phe224Cys
NM_002047.2:c.833T>G , LRG_243t1:c.833T>G	NP_002038.2:p.Phe278Cys
NM_002047.3:c.833T>G	NP_002038.2:p.Phe278Cys
XM_006715686.1:c.464T>G	XP_006715749.1:p.Phe155Cys
XM_006715686.2:c.464T>G	XP_006715749.1:p.Phe155Cys
NM_002047.4:c.833T>G MANE Select	NP_002038.2:p.Phe278Cys