Canonical Allele Identifier: CA417064439

Gene: YARS1

Linked Data

• MyVariant Identifiers: chr1:g.33245799T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780198T>A , CM000663.2:g.32780198T>A	GRCh38
NC_000001.10:g.33245799T>A , CM000663.1:g.33245799T>A	GRCh37
NC_000001.9:g.33018386T>A	NCBI36
NG_008408.1:g.42835A>T , LRG_273:g.42835A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1074A>T	ENSP00000502019.1:p.Val358=
ENST00000373477.9:c.1221A>T MANE Select	ENSP00000362576.4:p.Val407=
ENST00000674629.1:c.*769A>T	ENSP00000502470.1:n.*769A>T
ENST00000674654.1:c.*1181A>T	ENSP00000501729.1:n.*1181A>T
ENST00000675785.1:c.1074A>T	ENSP00000502019.1:p.Val358=
ENST00000676297.1:c.*1395A>T	ENSP00000501596.1:n.*1395A>T
ENST00000373477.8:c.1221A>T	ENSP00000362576.4:p.Val407=
ENST00000469100.5:n.1137A>T
ENST00000478828.1:n.688A>T
ENST00000487404.5:n.1531A>T
ENST00000490826.1:n.514A>T
NM_003680.3:c.1221A>T , LRG_273t1:c.1221A>T	NP_003671.1:p.Val407=
XM_011542347.1:c.591A>T	XP_011540649.1:p.Val197=
XM_011542348.1:c.591A>T	XP_011540650.1:p.Val197=
XM_011542347.2:c.591A>T	XP_011540649.1:p.Val197=
XM_017002651.2:c.591A>T	XP_016858140.1:p.Val197=
NM_003680.4:c.1221A>T MANE Select	NP_003671.1:p.Val407=