Canonical Allele Identifier: CA367124647

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30649322T>A (hg19) ; chr7:g.30609706T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30609706T>A , CM000669.2:g.30609706T>A	GRCh38
NC_000007.13:g.30649322T>A , CM000669.1:g.30649322T>A	GRCh37
NC_000007.12:g.30615847T>A	NCBI36
NG_007942.1:g.20142T>A , LRG_243:g.20142T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.857T>A MANE Select	ENSP00000373918.3:p.Ile286Asn
ENST00000444666.6:c.857T>A	ENSP00000415447.2:p.Ile286Asn
ENST00000470392.2:n.947T>A
ENST00000478124.6:n.920T>A
ENST00000485784.2:n.936T>A
ENST00000674616.1:c.*571T>A	ENSP00000502408.1:n.*571T>A
ENST00000674643.1:c.857T>A	ENSP00000501636.1:p.Ile286Asn
ENST00000674734.1:n.1353T>A
ENST00000674737.1:c.*195T>A	ENSP00000502464.1:n.*195T>A
ENST00000674807.1:c.857T>A	ENSP00000502814.1:p.Ile286Asn
ENST00000674815.1:c.488T>A	ENSP00000502799.1:p.Ile163Asn
ENST00000674851.1:c.488T>A	ENSP00000502451.1:p.Ile163Asn
ENST00000674969.1:n.2730T>A
ENST00000675051.1:c.656T>A	ENSP00000502296.1:p.Ile219Asn
ENST00000675529.1:c.*727T>A	ENSP00000501655.1:n.*727T>A
ENST00000675587.1:n.873T>A
ENST00000675651.1:c.857T>A	ENSP00000502513.1:p.Ile286Asn
ENST00000675693.1:c.689T>A	ENSP00000502174.1:p.Ile230Asn
ENST00000675810.1:c.755T>A	ENSP00000502743.1:p.Ile252Asn
ENST00000675859.1:c.857T>A	ENSP00000502033.1:p.Ile286Asn
ENST00000675863.1:n.865T>A
ENST00000675886.1:n.6897T>A
ENST00000676088.1:c.*799T>A	ENSP00000501884.1:n.*799T>A
ENST00000676140.1:c.857T>A	ENSP00000502571.1:p.Ile286Asn
ENST00000676164.1:c.*308T>A	ENSP00000501986.1:n.*308T>A
ENST00000676210.1:c.*146T>A	ENSP00000502373.1:n.*146T>A
ENST00000676259.1:c.*289T>A	ENSP00000501980.1:n.*289T>A
ENST00000676403.1:c.857T>A	ENSP00000502681.1:p.Ile286Asn
ENST00000389266.7:c.857T>A	ENSP00000373918.3:p.Ile286Asn
ENST00000478124.5:n.895T>A
NM_001316772.1:c.695T>A	NP_001303701.1:p.Ile232Asn
NM_002047.2:c.857T>A , LRG_243t1:c.857T>A	NP_002038.2:p.Ile286Asn
NM_002047.3:c.857T>A	NP_002038.2:p.Ile286Asn
XM_006715686.1:c.488T>A	XP_006715749.1:p.Ile163Asn
XM_006715686.2:c.488T>A	XP_006715749.1:p.Ile163Asn
NM_002047.4:c.857T>A MANE Select	NP_002038.2:p.Ile286Asn