Canonical Allele Identifier: CA1697777679

Gene: GARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30626116T= , CM000669.2:g.30626116T=	GRCh38
NC_000007.13:g.30665732T= , CM000669.1:g.30665732T=	GRCh37
NC_000007.12:g.30632257T=	NCBI36
NG_007942.1:g.36552T= , LRG_243:g.36552T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.1614-118T= MANE Select	ENSP00000373918.3:n.1614-118T=
ENST00000444666.6:c.1614-118T=	ENSP00000415447.2:n.1614-118T=
ENST00000470392.2:n.1704-118T=
ENST00000485784.2:n.1693-118T=
ENST00000674616.1:c.*1328-118T=	ENSP00000502408.1:n.*1328-118T=
ENST00000674643.1:c.*714-118T=	ENSP00000501636.1:n.*714-118T=
ENST00000674737.1:c.*952-118T=	ENSP00000502464.1:n.*952-118T=
ENST00000674807.1:c.1614-2444T=	ENSP00000502814.1:n.1614-2444T=
ENST00000674815.1:c.1245-118T=	ENSP00000502799.1:n.1245-118T=
ENST00000674851.1:c.1245-118T=	ENSP00000502451.1:n.1245-118T=
ENST00000674969.1:n.3487-118T=
ENST00000675051.1:c.1413-118T=	ENSP00000502296.1:n.1413-118T=
ENST00000675529.1:c.*1484-118T=	ENSP00000501655.1:n.*1484-118T=
ENST00000675587.1:n.2446-118T=
ENST00000675651.1:c.1614-118T=	ENSP00000502513.1:n.1614-118T=
ENST00000675693.1:c.1446-118T=	ENSP00000502174.1:n.1446-118T=
ENST00000675810.1:c.1512-118T=	ENSP00000502743.1:n.1512-118T=
ENST00000675859.1:c.1614-2444T=	ENSP00000502033.1:n.1614-2444T=
ENST00000675863.1:n.1622-118T=
ENST00000675886.1:n.7654-118T=
ENST00000676088.1:c.*1556-118T=	ENSP00000501884.1:n.*1556-118T=
ENST00000676140.1:c.*559-118T=	ENSP00000502571.1:n.*559-118T=
ENST00000676164.1:c.*1065-118T=	ENSP00000501986.1:n.*1065-118T=
ENST00000676210.1:c.*903-118T=	ENSP00000502373.1:n.*903-118T=
ENST00000676259.1:c.*1046-118T=	ENSP00000501980.1:n.*1046-118T=
ENST00000676403.1:c.1614-118T=	ENSP00000502681.1:n.1614-118T=
ENST00000389266.7:c.1614-118T=	ENSP00000373918.3:n.1614-118T=
ENST00000444666.5:c.135-118T=	ENSP00000415447.1:n.135-118T=
ENST00000470392.1:n.336-118T=
NM_001316772.1:c.1452-118T=	NP_001303701.1:n.1452-118T=
NM_002047.2:c.1614-118T= , LRG_243t1:c.1614-118T=	NP_002038.2:n.1614-118T=
NM_002047.3:c.1614-118T=	NP_002038.2:n.1614-118T=
XM_006715686.1:c.1245-118T=	XP_006715749.1:n.1245-118T=
XM_006715686.2:c.1245-118T=	XP_006715749.1:n.1245-118T=
NM_002047.4:c.1614-118T= MANE Select	NP_002038.2:n.1614-118T=