Canonical Allele Identifier: CA367129476

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30665932T>A (hg19) ; chr7:g.30626316T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30626316T>A , CM000669.2:g.30626316T>A	GRCh38
NC_000007.13:g.30665932T>A , CM000669.1:g.30665932T>A	GRCh37
NC_000007.12:g.30632457T>A	NCBI36
NG_007942.1:g.36752T>A , LRG_243:g.36752T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.1696T>A MANE Select	ENSP00000373918.3:p.Tyr566Asn
ENST00000444666.6:c.1696T>A	ENSP00000415447.2:p.Tyr566Asn
ENST00000470392.2:n.1786T>A
ENST00000485784.2:n.1775T>A
ENST00000674616.1:c.*1410T>A	ENSP00000502408.1:n.*1410T>A
ENST00000674643.1:c.*796T>A	ENSP00000501636.1:n.*796T>A
ENST00000674737.1:c.*1034T>A	ENSP00000502464.1:n.*1034T>A
ENST00000674807.1:c.1614-2244T>A	ENSP00000502814.1:n.1614-2244T>A
ENST00000674815.1:c.1327T>A	ENSP00000502799.1:p.Tyr443Asn
ENST00000674851.1:c.1327T>A	ENSP00000502451.1:p.Tyr443Asn
ENST00000674969.1:n.3569T>A
ENST00000675051.1:c.1495T>A	ENSP00000502296.1:p.Tyr499Asn
ENST00000675529.1:c.*1566T>A	ENSP00000501655.1:n.*1566T>A
ENST00000675587.1:n.2528T>A
ENST00000675651.1:c.1696T>A	ENSP00000502513.1:p.Tyr566Asn
ENST00000675693.1:c.1528T>A	ENSP00000502174.1:p.Tyr510Asn
ENST00000675810.1:c.1594T>A	ENSP00000502743.1:p.Tyr532Asn
ENST00000675859.1:c.1614-2244T>A	ENSP00000502033.1:n.1614-2244T>A
ENST00000675863.1:n.1704T>A
ENST00000675886.1:n.7736T>A
ENST00000676088.1:c.*1638T>A	ENSP00000501884.1:n.*1638T>A
ENST00000676140.1:c.*641T>A	ENSP00000502571.1:n.*641T>A
ENST00000676164.1:c.*1147T>A	ENSP00000501986.1:n.*1147T>A
ENST00000676210.1:c.*985T>A	ENSP00000502373.1:n.*985T>A
ENST00000676259.1:c.*1128T>A	ENSP00000501980.1:n.*1128T>A
ENST00000676403.1:c.1696T>A	ENSP00000502681.1:p.Tyr566Asn
ENST00000389266.7:c.1696T>A	ENSP00000373918.3:p.Tyr566Asn
ENST00000444666.5:c.217T>A	ENSP00000415447.1:p.Tyr73Asn
ENST00000470392.1:n.418T>A
NM_001316772.1:c.1534T>A	NP_001303701.1:p.Tyr512Asn
NM_002047.2:c.1696T>A , LRG_243t1:c.1696T>A	NP_002038.2:p.Tyr566Asn
NM_002047.3:c.1696T>A	NP_002038.2:p.Tyr566Asn
XM_006715686.1:c.1327T>A	XP_006715749.1:p.Tyr443Asn
XM_006715686.2:c.1327T>A	XP_006715749.1:p.Tyr443Asn
NM_002047.4:c.1696T>A MANE Select	NP_002038.2:p.Tyr566Asn