Canonical Allele Identifier: CA367124439

Gene: GARS1

Linked Data

• gnomAD v4: 7-30609658-A-G
• MyVariant Identifiers: chr7:g.30649274A>G (hg19) ; chr7:g.30609658A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30609658A>G , CM000669.2:g.30609658A>G	GRCh38
NC_000007.13:g.30649274A>G , CM000669.1:g.30649274A>G	GRCh37
NC_000007.12:g.30615799A>G	NCBI36
NG_007942.1:g.20094A>G , LRG_243:g.20094A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.809A>G MANE Select	ENSP00000373918.3:p.Asn270Ser
ENST00000444666.6:c.809A>G	ENSP00000415447.2:p.Asn270Ser
ENST00000470392.2:n.899A>G
ENST00000478124.6:n.872A>G
ENST00000485784.2:n.888A>G
ENST00000674616.1:c.*523A>G	ENSP00000502408.1:n.*523A>G
ENST00000674643.1:c.809A>G	ENSP00000501636.1:p.Asn270Ser
ENST00000674734.1:n.1305A>G
ENST00000674737.1:c.*147A>G	ENSP00000502464.1:n.*147A>G
ENST00000674807.1:c.809A>G	ENSP00000502814.1:p.Asn270Ser
ENST00000674815.1:c.440A>G	ENSP00000502799.1:p.Asn147Ser
ENST00000674851.1:c.440A>G	ENSP00000502451.1:p.Asn147Ser
ENST00000674969.1:n.2682A>G
ENST00000675051.1:c.608A>G	ENSP00000502296.1:p.Asn203Ser
ENST00000675529.1:c.*679A>G	ENSP00000501655.1:n.*679A>G
ENST00000675587.1:n.825A>G
ENST00000675651.1:c.809A>G	ENSP00000502513.1:p.Asn270Ser
ENST00000675693.1:c.641A>G	ENSP00000502174.1:p.Asn214Ser
ENST00000675810.1:c.707A>G	ENSP00000502743.1:p.Asn236Ser
ENST00000675859.1:c.809A>G	ENSP00000502033.1:p.Asn270Ser
ENST00000675863.1:n.817A>G
ENST00000675886.1:n.6849A>G
ENST00000676088.1:c.*751A>G	ENSP00000501884.1:n.*751A>G
ENST00000676140.1:c.809A>G	ENSP00000502571.1:p.Asn270Ser
ENST00000676164.1:c.*260A>G	ENSP00000501986.1:n.*260A>G
ENST00000676210.1:c.*98A>G	ENSP00000502373.1:n.*98A>G
ENST00000676259.1:c.*241A>G	ENSP00000501980.1:n.*241A>G
ENST00000676403.1:c.809A>G	ENSP00000502681.1:p.Asn270Ser
ENST00000389266.7:c.809A>G	ENSP00000373918.3:p.Asn270Ser
ENST00000478124.5:n.847A>G
NM_001316772.1:c.647A>G	NP_001303701.1:p.Asn216Ser
NM_002047.2:c.809A>G , LRG_243t1:c.809A>G	NP_002038.2:p.Asn270Ser
NM_002047.3:c.809A>G	NP_002038.2:p.Asn270Ser
XM_006715686.1:c.440A>G	XP_006715749.1:p.Asn147Ser
XM_006715686.2:c.440A>G	XP_006715749.1:p.Asn147Ser
NM_002047.4:c.809A>G MANE Select	NP_002038.2:p.Asn270Ser