Canonical Allele Identifier: CA2644702504

Gene: YARS1

Linked Data

• gnomAD v4: 1-32780201-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780201_32780202insG , CM000663.2:g.32780201_32780202insG	GRCh38
NC_000001.10:g.33245802_33245803insG , CM000663.1:g.33245802_33245803insG	GRCh37
NC_000001.9:g.33018389_33018390insG	NCBI36
NG_008408.1:g.42831_42832insC , LRG_273:g.42831_42832insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1070_1071insC	ENSP00000502019.1:p.Val358GlyfsTer?
ENST00000373477.9:c.1217_1218insC MANE Select	ENSP00000362576.4:p.Val407GlyfsTer?
ENST00000674629.1:c.*765_*766insC	ENSP00000502470.1:n.*765_*766insC
ENST00000674654.1:c.*1177_*1178insC	ENSP00000501729.1:n.*1177_*1178insC
ENST00000675785.1:c.1070_1071insC	ENSP00000502019.1:p.Val358GlyfsTer?
ENST00000676297.1:c.*1391_*1392insC	ENSP00000501596.1:n.*1391_*1392insC
ENST00000373477.8:c.1217_1218insC	ENSP00000362576.4:p.Val407GlyfsTer?
ENST00000469100.5:n.1133_1134insC
ENST00000478828.1:n.684_685insC
ENST00000487404.5:n.1527_1528insC
ENST00000490826.1:n.510_511insC
NM_003680.3:c.1217_1218insC , LRG_273t1:c.1217_1218insC	NP_003671.1:p.Val407GlyfsTer?
XM_011542347.1:c.587_588insC	XP_011540649.1:p.Val197GlyfsTer?
XM_011542348.1:c.587_588insC	XP_011540650.1:p.Val197GlyfsTer?
XM_011542347.2:c.587_588insC	XP_011540649.1:p.Val197GlyfsTer?
XM_017002651.2:c.587_588insC	XP_016858140.1:p.Val197GlyfsTer?
NM_003680.4:c.1217_1218insC MANE Select	NP_003671.1:p.Val407GlyfsTer?