Canonical Allele Identifier: CA2578858577

Gene: GARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612063C>A , CM000669.2:g.30612063C>A	GRCh38
NC_000007.13:g.30651679C>A , CM000669.1:g.30651679C>A	GRCh37
NC_000007.12:g.30618204C>A	NCBI36
NG_007942.1:g.22499C>A , LRG_243:g.22499C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.882-33C>A MANE Select	ENSP00000373918.3:n.882-33C>A
ENST00000444666.6:c.882-33C>A	ENSP00000415447.2:n.882-33C>A
ENST00000470392.2:n.972-33C>A
ENST00000478124.6:n.945-33C>A
ENST00000485784.2:n.961-33C>A
ENST00000674616.1:c.*596-33C>A	ENSP00000502408.1:n.*596-33C>A
ENST00000674643.1:c.882-33C>A	ENSP00000501636.1:n.882-33C>A
ENST00000674734.1:n.1378-33C>A
ENST00000674737.1:c.*220-33C>A	ENSP00000502464.1:n.*220-33C>A
ENST00000674807.1:c.882-33C>A	ENSP00000502814.1:n.882-33C>A
ENST00000674815.1:c.513-33C>A	ENSP00000502799.1:n.513-33C>A
ENST00000674851.1:c.513-33C>A	ENSP00000502451.1:n.513-33C>A
ENST00000674969.1:n.2755-33C>A
ENST00000675051.1:c.681-33C>A	ENSP00000502296.1:n.681-33C>A
ENST00000675529.1:c.*752-33C>A	ENSP00000501655.1:n.*752-33C>A
ENST00000675587.1:n.898-33C>A
ENST00000675651.1:c.882-33C>A	ENSP00000502513.1:n.882-33C>A
ENST00000675693.1:c.714-33C>A	ENSP00000502174.1:n.714-33C>A
ENST00000675810.1:c.780-33C>A	ENSP00000502743.1:n.780-33C>A
ENST00000675859.1:c.882-33C>A	ENSP00000502033.1:n.882-33C>A
ENST00000675863.1:n.890-33C>A
ENST00000675886.1:n.6922-33C>A
ENST00000676088.1:c.*824-33C>A	ENSP00000501884.1:n.*824-33C>A
ENST00000676140.1:c.882-33C>A	ENSP00000502571.1:n.882-33C>A
ENST00000676164.1:c.*333-33C>A	ENSP00000501986.1:n.*333-33C>A
ENST00000676210.1:c.*171-33C>A	ENSP00000502373.1:n.*171-33C>A
ENST00000676259.1:c.*314-33C>A	ENSP00000501980.1:n.*314-33C>A
ENST00000676403.1:c.882-33C>A	ENSP00000502681.1:n.882-33C>A
ENST00000389266.7:c.882-33C>A	ENSP00000373918.3:n.882-33C>A
ENST00000478124.5:n.920-33C>A
NM_001316772.1:c.720-33C>A	NP_001303701.1:n.720-33C>A
NM_002047.2:c.882-33C>A , LRG_243t1:c.882-33C>A	NP_002038.2:n.882-33C>A
NM_002047.3:c.882-33C>A	NP_002038.2:n.882-33C>A
XM_006715686.1:c.513-33C>A	XP_006715749.1:n.513-33C>A
XM_006715686.2:c.513-33C>A	XP_006715749.1:n.513-33C>A
NM_002047.4:c.882-33C>A MANE Select	NP_002038.2:n.882-33C>A