Canonical Allele Identifier: CA1697811131

Gene: GARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612194G= , CM000669.2:g.30612194G=	GRCh38
NC_000007.13:g.30651810G= , CM000669.1:g.30651810G=	GRCh37
NC_000007.12:g.30618335G=	NCBI36
NG_007942.1:g.22630G= , LRG_243:g.22630G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.980G= MANE Select	ENSP00000373918.3:p.Gly327=
ENST00000444666.6:c.980G=	ENSP00000415447.2:p.Gly327=
ENST00000470392.2:n.1070G=
ENST00000478124.6:n.1043G=
ENST00000485784.2:n.1059G=
ENST00000674616.1:c.*694G=	ENSP00000502408.1:n.*694G=
ENST00000674643.1:c.980G=	ENSP00000501636.1:p.Gly327=
ENST00000674734.1:n.1476G=
ENST00000674737.1:c.*318G=	ENSP00000502464.1:n.*318G=
ENST00000674807.1:c.980G=	ENSP00000502814.1:p.Gly327=
ENST00000674815.1:c.611G=	ENSP00000502799.1:p.Gly204=
ENST00000674851.1:c.611G=	ENSP00000502451.1:p.Gly204=
ENST00000674969.1:n.2853G=
ENST00000675051.1:c.779G=	ENSP00000502296.1:p.Gly260=
ENST00000675529.1:c.*850G=	ENSP00000501655.1:n.*850G=
ENST00000675587.1:n.996G=
ENST00000675651.1:c.980G=	ENSP00000502513.1:p.Gly327=
ENST00000675693.1:c.812G=	ENSP00000502174.1:p.Gly271=
ENST00000675810.1:c.878G=	ENSP00000502743.1:p.Gly293=
ENST00000675859.1:c.980G=	ENSP00000502033.1:p.Gly327=
ENST00000675863.1:n.988G=
ENST00000675886.1:n.7020G=
ENST00000676088.1:c.*922G=	ENSP00000501884.1:n.*922G=
ENST00000676140.1:c.980G=	ENSP00000502571.1:p.Gly327=
ENST00000676164.1:c.*431G=	ENSP00000501986.1:n.*431G=
ENST00000676210.1:c.*269G=	ENSP00000502373.1:n.*269G=
ENST00000676259.1:c.*412G=	ENSP00000501980.1:n.*412G=
ENST00000676403.1:c.980G=	ENSP00000502681.1:p.Gly327=
ENST00000389266.7:c.980G=	ENSP00000373918.3:p.Gly327=
ENST00000478124.5:n.1018G=
NM_001316772.1:c.818G=	NP_001303701.1:p.Gly273=
NM_002047.2:c.980G= , LRG_243t1:c.980G=	NP_002038.2:p.Gly327=
NM_002047.3:c.980G=	NP_002038.2:p.Gly327=
XM_006715686.1:c.611G=	XP_006715749.1:p.Gly204=
XM_006715686.2:c.611G=	XP_006715749.1:p.Gly204=
NM_002047.4:c.980G= MANE Select	NP_002038.2:p.Gly327=