Canonical Allele Identifier: CA20273882

Gene: YARS1

Linked Data

• ClinVar Variation Id: 1904618
• ClinVar RCV Id: RCV002592734
• dbSNP Id: rs569727346
• gnomAD v3: 1-32780197-G-A
• gnomAD v4: 1-32780197-G-A
• MyVariant Identifiers: chr1:g.33245798G>A (hg19) ; chr1:g.32780197G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780197G>A , CM000663.2:g.32780197G>A	GRCh38
NC_000001.10:g.33245798G>A , CM000663.1:g.33245798G>A	GRCh37
NC_000001.9:g.33018385G>A	NCBI36
NG_008408.1:g.42836C>T , LRG_273:g.42836C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1075C>T	ENSP00000502019.1:p.Gln359Ter
ENST00000373477.9:c.1222C>T MANE Select	ENSP00000362576.4:p.Gln408Ter
ENST00000674629.1:c.*770C>T	ENSP00000502470.1:n.*770C>T
ENST00000674654.1:c.*1182C>T	ENSP00000501729.1:n.*1182C>T
ENST00000675785.1:c.1075C>T	ENSP00000502019.1:p.Gln359Ter
ENST00000676297.1:c.*1396C>T	ENSP00000501596.1:n.*1396C>T
ENST00000373477.8:c.1222C>T	ENSP00000362576.4:p.Gln408Ter
ENST00000469100.5:n.1138C>T
ENST00000478828.1:n.689C>T
ENST00000487404.5:n.1532C>T
ENST00000490826.1:n.515C>T
NM_003680.3:c.1222C>T , LRG_273t1:c.1222C>T	NP_003671.1:p.Gln408Ter
XM_011542347.1:c.592C>T	XP_011540649.1:p.Gln198Ter
XM_011542348.1:c.592C>T	XP_011540650.1:p.Gln198Ter
XM_011542347.2:c.592C>T	XP_011540649.1:p.Gln198Ter
XM_017002651.2:c.592C>T	XP_016858140.1:p.Gln198Ter
NM_003680.4:c.1222C>T MANE Select	NP_003671.1:p.Gln408Ter