Canonical Allele Identifier: CA454247102

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30651817T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612201T>A , CM000669.2:g.30612201T>A	GRCh38
NC_000007.13:g.30651817T>A , CM000669.1:g.30651817T>A	GRCh37
NC_000007.12:g.30618342T>A	NCBI36
NG_007942.1:g.22637T>A , LRG_243:g.22637T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.987T>A MANE Select	ENSP00000373918.3:p.Ser329=
ENST00000444666.6:c.987T>A	ENSP00000415447.2:p.Ser329=
ENST00000470392.2:n.1077T>A
ENST00000478124.6:n.1050T>A
ENST00000485784.2:n.1066T>A
ENST00000674616.1:c.*701T>A	ENSP00000502408.1:n.*701T>A
ENST00000674643.1:c.987T>A	ENSP00000501636.1:p.Ser329=
ENST00000674734.1:n.1483T>A
ENST00000674737.1:c.*325T>A	ENSP00000502464.1:n.*325T>A
ENST00000674807.1:c.987T>A	ENSP00000502814.1:p.Ser329=
ENST00000674815.1:c.618T>A	ENSP00000502799.1:p.Ser206=
ENST00000674851.1:c.618T>A	ENSP00000502451.1:p.Ser206=
ENST00000674969.1:n.2860T>A
ENST00000675051.1:c.786T>A	ENSP00000502296.1:p.Ser262=
ENST00000675529.1:c.*857T>A	ENSP00000501655.1:n.*857T>A
ENST00000675587.1:n.1003T>A
ENST00000675651.1:c.987T>A	ENSP00000502513.1:p.Ser329=
ENST00000675693.1:c.819T>A	ENSP00000502174.1:p.Ser273=
ENST00000675810.1:c.885T>A	ENSP00000502743.1:p.Ser295=
ENST00000675859.1:c.987T>A	ENSP00000502033.1:p.Ser329=
ENST00000675863.1:n.995T>A
ENST00000675886.1:n.7027T>A
ENST00000676088.1:c.*929T>A	ENSP00000501884.1:n.*929T>A
ENST00000676140.1:c.987T>A	ENSP00000502571.1:p.Ser329=
ENST00000676164.1:c.*438T>A	ENSP00000501986.1:n.*438T>A
ENST00000676210.1:c.*276T>A	ENSP00000502373.1:n.*276T>A
ENST00000676259.1:c.*419T>A	ENSP00000501980.1:n.*419T>A
ENST00000676403.1:c.987T>A	ENSP00000502681.1:p.Ser329=
ENST00000389266.7:c.987T>A	ENSP00000373918.3:p.Ser329=
ENST00000478124.5:n.1025T>A
NM_001316772.1:c.825T>A	NP_001303701.1:p.Ser275=
NM_002047.2:c.987T>A , LRG_243t1:c.987T>A	NP_002038.2:p.Ser329=
NM_002047.3:c.987T>A	NP_002038.2:p.Ser329=
XM_006715686.1:c.618T>A	XP_006715749.1:p.Ser206=
XM_006715686.2:c.618T>A	XP_006715749.1:p.Ser206=
NM_002047.4:c.987T>A MANE Select	NP_002038.2:p.Ser329=