Canonical Allele Identifier: CA367128256

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30661080A>T (hg19) ; chr7:g.30621464A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30621464A>T , CM000669.2:g.30621464A>T	GRCh38
NC_000007.13:g.30661080A>T , CM000669.1:g.30661080A>T	GRCh37
NC_000007.12:g.30627605A>T	NCBI36
NG_007942.1:g.31900A>T , LRG_243:g.31900A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.1431A>T MANE Select	ENSP00000373918.3:p.Lys477Asn
ENST00000444666.6:c.1431A>T	ENSP00000415447.2:p.Lys477Asn
ENST00000470392.2:n.1521A>T
ENST00000478124.6:n.1494A>T
ENST00000485784.2:n.1510A>T
ENST00000674616.1:c.*1145A>T	ENSP00000502408.1:n.*1145A>T
ENST00000674643.1:c.*531A>T	ENSP00000501636.1:n.*531A>T
ENST00000674734.1:n.1927A>T
ENST00000674737.1:c.*769A>T	ENSP00000502464.1:n.*769A>T
ENST00000674807.1:c.1431A>T	ENSP00000502814.1:p.Lys477Asn
ENST00000674815.1:c.1062A>T	ENSP00000502799.1:p.Lys354Asn
ENST00000674851.1:c.1062A>T	ENSP00000502451.1:p.Lys354Asn
ENST00000674969.1:n.3304A>T
ENST00000675051.1:c.1230A>T	ENSP00000502296.1:p.Lys410Asn
ENST00000675529.1:c.*1301A>T	ENSP00000501655.1:n.*1301A>T
ENST00000675587.1:n.1447A>T
ENST00000675651.1:c.1431A>T	ENSP00000502513.1:p.Lys477Asn
ENST00000675693.1:c.1263A>T	ENSP00000502174.1:p.Lys421Asn
ENST00000675810.1:c.1329A>T	ENSP00000502743.1:p.Lys443Asn
ENST00000675859.1:c.1431A>T	ENSP00000502033.1:p.Lys477Asn
ENST00000675863.1:n.1439A>T
ENST00000675886.1:n.7471A>T
ENST00000676088.1:c.*1373A>T	ENSP00000501884.1:n.*1373A>T
ENST00000676140.1:c.*376A>T	ENSP00000502571.1:n.*376A>T
ENST00000676164.1:c.*882A>T	ENSP00000501986.1:n.*882A>T
ENST00000676210.1:c.*720A>T	ENSP00000502373.1:n.*720A>T
ENST00000676259.1:c.*863A>T	ENSP00000501980.1:n.*863A>T
ENST00000676403.1:c.1431A>T	ENSP00000502681.1:p.Lys477Asn
ENST00000389266.7:c.1431A>T	ENSP00000373918.3:p.Lys477Asn
ENST00000478124.5:n.1469A>T
ENST00000484093.1:n.430A>T
NM_001316772.1:c.1269A>T	NP_001303701.1:p.Lys423Asn
NM_002047.2:c.1431A>T , LRG_243t1:c.1431A>T	NP_002038.2:p.Lys477Asn
NM_002047.3:c.1431A>T	NP_002038.2:p.Lys477Asn
XM_006715686.1:c.1062A>T	XP_006715749.1:p.Lys354Asn
XM_006715686.2:c.1062A>T	XP_006715749.1:p.Lys354Asn
NM_002047.4:c.1431A>T MANE Select	NP_002038.2:p.Lys477Asn