Canonical Allele Identifier: CA367125152

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30651807T>A (hg19) ; chr7:g.30612191T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612191T>A , CM000669.2:g.30612191T>A	GRCh38
NC_000007.13:g.30651807T>A , CM000669.1:g.30651807T>A	GRCh37
NC_000007.12:g.30618332T>A	NCBI36
NG_007942.1:g.22627T>A , LRG_243:g.22627T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.977T>A MANE Select	ENSP00000373918.3:p.Ile326Asn
ENST00000444666.6:c.977T>A	ENSP00000415447.2:p.Ile326Asn
ENST00000470392.2:n.1067T>A
ENST00000478124.6:n.1040T>A
ENST00000485784.2:n.1056T>A
ENST00000674616.1:c.*691T>A	ENSP00000502408.1:n.*691T>A
ENST00000674643.1:c.977T>A	ENSP00000501636.1:p.Ile326Asn
ENST00000674734.1:n.1473T>A
ENST00000674737.1:c.*315T>A	ENSP00000502464.1:n.*315T>A
ENST00000674807.1:c.977T>A	ENSP00000502814.1:p.Ile326Asn
ENST00000674815.1:c.608T>A	ENSP00000502799.1:p.Ile203Asn
ENST00000674851.1:c.608T>A	ENSP00000502451.1:p.Ile203Asn
ENST00000674969.1:n.2850T>A
ENST00000675051.1:c.776T>A	ENSP00000502296.1:p.Ile259Asn
ENST00000675529.1:c.*847T>A	ENSP00000501655.1:n.*847T>A
ENST00000675587.1:n.993T>A
ENST00000675651.1:c.977T>A	ENSP00000502513.1:p.Ile326Asn
ENST00000675693.1:c.809T>A	ENSP00000502174.1:p.Ile270Asn
ENST00000675810.1:c.875T>A	ENSP00000502743.1:p.Ile292Asn
ENST00000675859.1:c.977T>A	ENSP00000502033.1:p.Ile326Asn
ENST00000675863.1:n.985T>A
ENST00000675886.1:n.7017T>A
ENST00000676088.1:c.*919T>A	ENSP00000501884.1:n.*919T>A
ENST00000676140.1:c.977T>A	ENSP00000502571.1:p.Ile326Asn
ENST00000676164.1:c.*428T>A	ENSP00000501986.1:n.*428T>A
ENST00000676210.1:c.*266T>A	ENSP00000502373.1:n.*266T>A
ENST00000676259.1:c.*409T>A	ENSP00000501980.1:n.*409T>A
ENST00000676403.1:c.977T>A	ENSP00000502681.1:p.Ile326Asn
ENST00000389266.7:c.977T>A	ENSP00000373918.3:p.Ile326Asn
ENST00000478124.5:n.1015T>A
NM_001316772.1:c.815T>A	NP_001303701.1:p.Ile272Asn
NM_002047.2:c.977T>A , LRG_243t1:c.977T>A	NP_002038.2:p.Ile326Asn
NM_002047.3:c.977T>A	NP_002038.2:p.Ile326Asn
XM_006715686.1:c.608T>A	XP_006715749.1:p.Ile203Asn
XM_006715686.2:c.608T>A	XP_006715749.1:p.Ile203Asn
NM_002047.4:c.977T>A MANE Select	NP_002038.2:p.Ile326Asn