Canonical Allele Identifier: CA367128126

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30661052A>T (hg19) ; chr7:g.30621436A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30621436A>T , CM000669.2:g.30621436A>T	GRCh38
NC_000007.13:g.30661052A>T , CM000669.1:g.30661052A>T	GRCh37
NC_000007.12:g.30627577A>T	NCBI36
NG_007942.1:g.31872A>T , LRG_243:g.31872A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.1403A>T MANE Select	ENSP00000373918.3:p.Asp468Val
ENST00000444666.6:c.1403A>T	ENSP00000415447.2:p.Asp468Val
ENST00000470392.2:n.1493A>T
ENST00000478124.6:n.1466A>T
ENST00000485784.2:n.1482A>T
ENST00000674616.1:c.*1117A>T	ENSP00000502408.1:n.*1117A>T
ENST00000674643.1:c.*503A>T	ENSP00000501636.1:n.*503A>T
ENST00000674734.1:n.1899A>T
ENST00000674737.1:c.*741A>T	ENSP00000502464.1:n.*741A>T
ENST00000674807.1:c.1403A>T	ENSP00000502814.1:p.Asp468Val
ENST00000674815.1:c.1034A>T	ENSP00000502799.1:p.Asp345Val
ENST00000674851.1:c.1034A>T	ENSP00000502451.1:p.Asp345Val
ENST00000674969.1:n.3276A>T
ENST00000675051.1:c.1202A>T	ENSP00000502296.1:p.Asp401Val
ENST00000675529.1:c.*1273A>T	ENSP00000501655.1:n.*1273A>T
ENST00000675587.1:n.1419A>T
ENST00000675651.1:c.1403A>T	ENSP00000502513.1:p.Asp468Val
ENST00000675693.1:c.1235A>T	ENSP00000502174.1:p.Asp412Val
ENST00000675810.1:c.1301A>T	ENSP00000502743.1:p.Asp434Val
ENST00000675859.1:c.1403A>T	ENSP00000502033.1:p.Asp468Val
ENST00000675863.1:n.1411A>T
ENST00000675886.1:n.7443A>T
ENST00000676088.1:c.*1345A>T	ENSP00000501884.1:n.*1345A>T
ENST00000676140.1:c.*348A>T	ENSP00000502571.1:n.*348A>T
ENST00000676164.1:c.*854A>T	ENSP00000501986.1:n.*854A>T
ENST00000676210.1:c.*692A>T	ENSP00000502373.1:n.*692A>T
ENST00000676259.1:c.*835A>T	ENSP00000501980.1:n.*835A>T
ENST00000676403.1:c.1403A>T	ENSP00000502681.1:p.Asp468Val
ENST00000389266.7:c.1403A>T	ENSP00000373918.3:p.Asp468Val
ENST00000478124.5:n.1441A>T
ENST00000484093.1:n.402A>T
NM_001316772.1:c.1241A>T	NP_001303701.1:p.Asp414Val
NM_002047.2:c.1403A>T , LRG_243t1:c.1403A>T	NP_002038.2:p.Asp468Val
NM_002047.3:c.1403A>T	NP_002038.2:p.Asp468Val
XM_006715686.1:c.1034A>T	XP_006715749.1:p.Asp345Val
XM_006715686.2:c.1034A>T	XP_006715749.1:p.Asp345Val
NM_002047.4:c.1403A>T MANE Select	NP_002038.2:p.Asp468Val