Canonical Allele Identifier: CA367124812

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30651715C>A (hg19) ; chr7:g.30612099C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30612099C>A , CM000669.2:g.30612099C>A	GRCh38
NC_000007.13:g.30651715C>A , CM000669.1:g.30651715C>A	GRCh37
NC_000007.12:g.30618240C>A	NCBI36
NG_007942.1:g.22535C>A , LRG_243:g.22535C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000389266.8:c.885C>A MANE Select	ENSP00000373918.3:p.Tyr295Ter
ENST00000444666.6:c.885C>A	ENSP00000415447.2:p.Tyr295Ter
ENST00000470392.2:n.975C>A
ENST00000478124.6:n.948C>A
ENST00000485784.2:n.964C>A
ENST00000674616.1:c.*599C>A	ENSP00000502408.1:n.*599C>A
ENST00000674643.1:c.885C>A	ENSP00000501636.1:p.Tyr295Ter
ENST00000674734.1:n.1381C>A
ENST00000674737.1:c.*223C>A	ENSP00000502464.1:n.*223C>A
ENST00000674807.1:c.885C>A	ENSP00000502814.1:p.Tyr295Ter
ENST00000674815.1:c.516C>A	ENSP00000502799.1:p.Tyr172Ter
ENST00000674851.1:c.516C>A	ENSP00000502451.1:p.Tyr172Ter
ENST00000674969.1:n.2758C>A
ENST00000675051.1:c.684C>A	ENSP00000502296.1:p.Tyr228Ter
ENST00000675529.1:c.*755C>A	ENSP00000501655.1:n.*755C>A
ENST00000675587.1:n.901C>A
ENST00000675651.1:c.885C>A	ENSP00000502513.1:p.Tyr295Ter
ENST00000675693.1:c.717C>A	ENSP00000502174.1:p.Tyr239Ter
ENST00000675810.1:c.783C>A	ENSP00000502743.1:p.Tyr261Ter
ENST00000675859.1:c.885C>A	ENSP00000502033.1:p.Tyr295Ter
ENST00000675863.1:n.893C>A
ENST00000675886.1:n.6925C>A
ENST00000676088.1:c.*827C>A	ENSP00000501884.1:n.*827C>A
ENST00000676140.1:c.885C>A	ENSP00000502571.1:p.Tyr295Ter
ENST00000676164.1:c.*336C>A	ENSP00000501986.1:n.*336C>A
ENST00000676210.1:c.*174C>A	ENSP00000502373.1:n.*174C>A
ENST00000676259.1:c.*317C>A	ENSP00000501980.1:n.*317C>A
ENST00000676403.1:c.885C>A	ENSP00000502681.1:p.Tyr295Ter
ENST00000389266.7:c.885C>A	ENSP00000373918.3:p.Tyr295Ter
ENST00000478124.5:n.923C>A
NM_001316772.1:c.723C>A	NP_001303701.1:p.Tyr241Ter
NM_002047.2:c.885C>A , LRG_243t1:c.885C>A	NP_002038.2:p.Tyr295Ter
NM_002047.3:c.885C>A	NP_002038.2:p.Tyr295Ter
XM_006715686.1:c.516C>A	XP_006715749.1:p.Tyr172Ter
XM_006715686.2:c.516C>A	XP_006715749.1:p.Tyr172Ter
NM_002047.4:c.885C>A MANE Select	NP_002038.2:p.Tyr295Ter