Canonical Allele Identifier: CA367124361

Gene: GARS1

Linked Data

• MyVariant Identifiers: chr7:g.30649261C>A (hg19) ; chr7:g.30609645C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.30609645C>A , CM000669.2:g.30609645C>A	GRCh38
NC_000007.13:g.30649261C>A , CM000669.1:g.30649261C>A	GRCh37
NC_000007.12:g.30615786C>A	NCBI36
NG_007942.1:g.20081C>A , LRG_243:g.20081C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389266.8:c.796C>A MANE Select	ENSP00000373918.3:p.Pro266Thr
ENST00000444666.6:c.796C>A	ENSP00000415447.2:p.Pro266Thr
ENST00000470392.2:n.886C>A
ENST00000478124.6:n.859C>A
ENST00000485784.2:n.875C>A
ENST00000674616.1:c.*510C>A	ENSP00000502408.1:n.*510C>A
ENST00000674643.1:c.796C>A	ENSP00000501636.1:p.Pro266Thr
ENST00000674734.1:n.1292C>A
ENST00000674737.1:c.*134C>A	ENSP00000502464.1:n.*134C>A
ENST00000674807.1:c.796C>A	ENSP00000502814.1:p.Pro266Thr
ENST00000674815.1:c.427C>A	ENSP00000502799.1:p.Pro143Thr
ENST00000674851.1:c.427C>A	ENSP00000502451.1:p.Pro143Thr
ENST00000674969.1:n.2669C>A
ENST00000675051.1:c.595C>A	ENSP00000502296.1:p.Pro199Thr
ENST00000675529.1:c.*666C>A	ENSP00000501655.1:n.*666C>A
ENST00000675587.1:n.812C>A
ENST00000675651.1:c.796C>A	ENSP00000502513.1:p.Pro266Thr
ENST00000675693.1:c.628C>A	ENSP00000502174.1:p.Pro210Thr
ENST00000675810.1:c.694C>A	ENSP00000502743.1:p.Pro232Thr
ENST00000675859.1:c.796C>A	ENSP00000502033.1:p.Pro266Thr
ENST00000675863.1:n.804C>A
ENST00000675886.1:n.6836C>A
ENST00000676088.1:c.*738C>A	ENSP00000501884.1:n.*738C>A
ENST00000676140.1:c.796C>A	ENSP00000502571.1:p.Pro266Thr
ENST00000676164.1:c.*247C>A	ENSP00000501986.1:n.*247C>A
ENST00000676210.1:c.*85C>A	ENSP00000502373.1:n.*85C>A
ENST00000676259.1:c.*228C>A	ENSP00000501980.1:n.*228C>A
ENST00000676403.1:c.796C>A	ENSP00000502681.1:p.Pro266Thr
ENST00000389266.7:c.796C>A	ENSP00000373918.3:p.Pro266Thr
ENST00000478124.5:n.834C>A
NM_001316772.1:c.634C>A	NP_001303701.1:p.Pro212Thr
NM_002047.2:c.796C>A , LRG_243t1:c.796C>A	NP_002038.2:p.Pro266Thr
NM_002047.3:c.796C>A	NP_002038.2:p.Pro266Thr
XM_006715686.1:c.427C>A	XP_006715749.1:p.Pro143Thr
XM_006715686.2:c.427C>A	XP_006715749.1:p.Pro143Thr
NM_002047.4:c.796C>A MANE Select	NP_002038.2:p.Pro266Thr