Canonical Allele Identifier: CA454518939

Gene: GARS1

Linked Data

• gnomAD v4: 7-30595134-G-A
• MyVariant Identifiers: chr7:g.30634750G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30595134G>A , CM000669.2:g.30595134G>A	GRCh38
NC_000007.13:g.30634750G>A , CM000669.1:g.30634750G>A	GRCh37
NC_000007.12:g.30601275G>A	NCBI36
NG_007942.1:g.5570G>A , LRG_243:g.5570G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.213G>A MANE Select	ENSP00000373918.3:p.Val71=
ENST00000444666.6:c.213G>A	ENSP00000415447.2:p.Val71=
ENST00000454308.6:c.213G>A	ENSP00000392677.2:p.Val71=
ENST00000470392.2:n.303G>A
ENST00000478124.6:n.276G>A
ENST00000485784.2:n.292G>A
ENST00000674616.1:c.213G>A	ENSP00000502408.1:p.Val71=
ENST00000674643.1:c.213G>A	ENSP00000501636.1:p.Val71=
ENST00000674737.1:c.213G>A	ENSP00000502464.1:p.Val71=
ENST00000674807.1:c.213G>A	ENSP00000502814.1:p.Val71=
ENST00000674815.1:c.-148+182G>A	ENSP00000502799.1:n.-148+182G>A
ENST00000674851.1:c.-157G>A	ENSP00000502451.1:n.-157G>A
ENST00000674969.1:n.253G>A
ENST00000675051.1:c.22-3662G>A	ENSP00000502296.1:n.22-3662G>A
ENST00000675529.1:c.213G>A	ENSP00000501655.1:p.Val71=
ENST00000675587.1:n.229G>A
ENST00000675651.1:c.213G>A	ENSP00000502513.1:p.Val71=
ENST00000675693.1:c.45G>A	ENSP00000502174.1:p.Val15=
ENST00000675810.1:c.213G>A	ENSP00000502743.1:p.Val71=
ENST00000675859.1:c.213G>A	ENSP00000502033.1:p.Val71=
ENST00000675863.1:n.221G>A
ENST00000675886.1:n.241G>A
ENST00000676088.1:c.213G>A	ENSP00000501884.1:p.Val71=
ENST00000676140.1:c.213G>A	ENSP00000502571.1:p.Val71=
ENST00000676164.1:c.213G>A	ENSP00000501986.1:p.Val71=
ENST00000676210.1:c.213G>A	ENSP00000502373.1:p.Val71=
ENST00000676259.1:c.213G>A	ENSP00000501980.1:p.Val71=
ENST00000676403.1:c.213G>A	ENSP00000502681.1:p.Val71=
ENST00000389266.7:c.213G>A	ENSP00000373918.3:p.Val71=
ENST00000454308.5:c.213G>A	ENSP00000392677.1:p.Val71=
ENST00000478124.5:n.251G>A
ENST00000627489.1:c.213G>A	ENSP00000485931.1:p.Val71=
NM_001316772.1:c.51G>A	NP_001303701.1:p.Val17=
NM_002047.2:c.213G>A , LRG_243t1:c.213G>A	NP_002038.2:p.Val71=
NM_002047.3:c.213G>A	NP_002038.2:p.Val71=
XM_006715686.2:c.-267G>A	XP_006715749.1:n.-267G>A
NM_002047.4:c.213G>A MANE Select	NP_002038.2:p.Val71=