Canonical Allele Identifier: CA367124455

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30649277A>T (hg19) ; chr7:g.30609661A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30609661A>T , CM000669.2:g.30609661A>T	GRCh38
NC_000007.13:g.30649277A>T , CM000669.1:g.30649277A>T	GRCh37
NC_000007.12:g.30615802A>T	NCBI36
NG_007942.1:g.20097A>T , LRG_243:g.20097A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.812A>T MANE Select	ENSP00000373918.3:p.Asp271Val
ENST00000444666.6:c.812A>T	ENSP00000415447.2:p.Asp271Val
ENST00000470392.2:n.902A>T
ENST00000478124.6:n.875A>T
ENST00000485784.2:n.891A>T
ENST00000674616.1:c.*526A>T	ENSP00000502408.1:n.*526A>T
ENST00000674643.1:c.812A>T	ENSP00000501636.1:p.Asp271Val
ENST00000674734.1:n.1308A>T
ENST00000674737.1:c.*150A>T	ENSP00000502464.1:n.*150A>T
ENST00000674807.1:c.812A>T	ENSP00000502814.1:p.Asp271Val
ENST00000674815.1:c.443A>T	ENSP00000502799.1:p.Asp148Val
ENST00000674851.1:c.443A>T	ENSP00000502451.1:p.Asp148Val
ENST00000674969.1:n.2685A>T
ENST00000675051.1:c.611A>T	ENSP00000502296.1:p.Asp204Val
ENST00000675529.1:c.*682A>T	ENSP00000501655.1:n.*682A>T
ENST00000675587.1:n.828A>T
ENST00000675651.1:c.812A>T	ENSP00000502513.1:p.Asp271Val
ENST00000675693.1:c.644A>T	ENSP00000502174.1:p.Asp215Val
ENST00000675810.1:c.710A>T	ENSP00000502743.1:p.Asp237Val
ENST00000675859.1:c.812A>T	ENSP00000502033.1:p.Asp271Val
ENST00000675863.1:n.820A>T
ENST00000675886.1:n.6852A>T
ENST00000676088.1:c.*754A>T	ENSP00000501884.1:n.*754A>T
ENST00000676140.1:c.812A>T	ENSP00000502571.1:p.Asp271Val
ENST00000676164.1:c.*263A>T	ENSP00000501986.1:n.*263A>T
ENST00000676210.1:c.*101A>T	ENSP00000502373.1:n.*101A>T
ENST00000676259.1:c.*244A>T	ENSP00000501980.1:n.*244A>T
ENST00000676403.1:c.812A>T	ENSP00000502681.1:p.Asp271Val
ENST00000389266.7:c.812A>T	ENSP00000373918.3:p.Asp271Val
ENST00000478124.5:n.850A>T
NM_001316772.1:c.650A>T	NP_001303701.1:p.Asp217Val
NM_002047.2:c.812A>T , LRG_243t1:c.812A>T	NP_002038.2:p.Asp271Val
NM_002047.3:c.812A>T	NP_002038.2:p.Asp271Val
XM_006715686.1:c.443A>T	XP_006715749.1:p.Asp148Val
XM_006715686.2:c.443A>T	XP_006715749.1:p.Asp148Val
NM_002047.4:c.812A>T MANE Select	NP_002038.2:p.Asp271Val