Canonical Allele Identifier: CA2473063200

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780237C= , CM000663.2:g.32780237C=	GRCh38
NC_000001.10:g.33245838C= , CM000663.1:g.33245838C=	GRCh37
NC_000001.9:g.33018425C=	NCBI36
NG_008408.1:g.42796G= , LRG_273:g.42796G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1035G=	ENSP00000502019.1:p.Val345=
ENST00000373477.9:c.1182G= MANE Select	ENSP00000362576.4:p.Val394=
ENST00000674629.1:c.*730G=	ENSP00000502470.1:n.*730G=
ENST00000674654.1:c.*1142G=	ENSP00000501729.1:n.*1142G=
ENST00000675785.1:c.1035G=	ENSP00000502019.1:p.Val345=
ENST00000676297.1:c.*1356G=	ENSP00000501596.1:n.*1356G=
ENST00000373477.8:c.1182G=	ENSP00000362576.4:p.Val394=
ENST00000469100.5:n.1098G=
ENST00000478828.1:n.649G=
ENST00000487404.5:n.1492G=
ENST00000490826.1:n.475G=
NM_003680.3:c.1182G= , LRG_273t1:c.1182G=	NP_003671.1:p.Val394=
XM_011542347.1:c.552G=	XP_011540649.1:p.Val184=
XM_011542348.1:c.552G=	XP_011540650.1:p.Val184=
XM_011542347.2:c.552G=	XP_011540649.1:p.Val184=
XM_017002651.2:c.552G=	XP_016858140.1:p.Val184=
NM_003680.4:c.1182G= MANE Select	NP_003671.1:p.Val394=