Canonical Allele Identifier: CA1697769845

Gene: GARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30621538A= , CM000669.2:g.30621538A=	GRCh38
NC_000007.13:g.30661154A= , CM000669.1:g.30661154A=	GRCh37
NC_000007.12:g.30627679A=	NCBI36
NG_007942.1:g.31974A= , LRG_243:g.31974A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.1467+38A= MANE Select	ENSP00000373918.3:n.1467+38A=
ENST00000444666.6:c.1467+38A=	ENSP00000415447.2:n.1467+38A=
ENST00000470392.2:n.1557+38A=
ENST00000478124.6:n.1530+38A=
ENST00000485784.2:n.1546+38A=
ENST00000674616.1:c.*1181+38A=	ENSP00000502408.1:n.*1181+38A=
ENST00000674643.1:c.*567+38A=	ENSP00000501636.1:n.*567+38A=
ENST00000674734.1:n.2001A=
ENST00000674737.1:c.*805+38A=	ENSP00000502464.1:n.*805+38A=
ENST00000674807.1:c.1467+38A=	ENSP00000502814.1:n.1467+38A=
ENST00000674815.1:c.1098+38A=	ENSP00000502799.1:n.1098+38A=
ENST00000674851.1:c.1098+38A=	ENSP00000502451.1:n.1098+38A=
ENST00000674969.1:n.3340+38A=
ENST00000675051.1:c.1266+38A=	ENSP00000502296.1:n.1266+38A=
ENST00000675529.1:c.*1337+38A=	ENSP00000501655.1:n.*1337+38A=
ENST00000675587.1:n.1521A=
ENST00000675651.1:c.1467+38A=	ENSP00000502513.1:n.1467+38A=
ENST00000675693.1:c.1299+38A=	ENSP00000502174.1:n.1299+38A=
ENST00000675810.1:c.1365+38A=	ENSP00000502743.1:n.1365+38A=
ENST00000675859.1:c.1467+38A=	ENSP00000502033.1:n.1467+38A=
ENST00000675863.1:n.1475+38A=
ENST00000675886.1:n.7507+38A=
ENST00000676088.1:c.*1409+38A=	ENSP00000501884.1:n.*1409+38A=
ENST00000676140.1:c.*412+38A=	ENSP00000502571.1:n.*412+38A=
ENST00000676164.1:c.*918+38A=	ENSP00000501986.1:n.*918+38A=
ENST00000676210.1:c.*756+38A=	ENSP00000502373.1:n.*756+38A=
ENST00000676259.1:c.*899+38A=	ENSP00000501980.1:n.*899+38A=
ENST00000676403.1:c.1467+38A=	ENSP00000502681.1:n.1467+38A=
ENST00000389266.7:c.1467+38A=	ENSP00000373918.3:n.1467+38A=
ENST00000478124.5:n.1505+38A=
ENST00000484093.1:n.504A=
NM_001316772.1:c.1305+38A=	NP_001303701.1:n.1305+38A=
NM_002047.2:c.1467+38A= , LRG_243t1:c.1467+38A=	NP_002038.2:n.1467+38A=
NM_002047.3:c.1467+38A=	NP_002038.2:n.1467+38A=
XM_006715686.1:c.1098+38A=	XP_006715749.1:n.1098+38A=
XM_006715686.2:c.1098+38A=	XP_006715749.1:n.1098+38A=
NM_002047.4:c.1467+38A= MANE Select	NP_002038.2:n.1467+38A=