Canonical Allele Identifier: CA2473063192

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780217G= , CM000663.2:g.32780217G=	GRCh38
NC_000001.10:g.33245818G= , CM000663.1:g.33245818G=	GRCh37
NC_000001.9:g.33018405G=	NCBI36
NG_008408.1:g.42816C= , LRG_273:g.42816C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1055C=	ENSP00000502019.1:p.Thr352=
ENST00000373477.9:c.1202C= MANE Select	ENSP00000362576.4:p.Thr401=
ENST00000674629.1:c.*750C=	ENSP00000502470.1:n.*750C=
ENST00000674654.1:c.*1162C=	ENSP00000501729.1:n.*1162C=
ENST00000675785.1:c.1055C=	ENSP00000502019.1:p.Thr352=
ENST00000676297.1:c.*1376C=	ENSP00000501596.1:n.*1376C=
ENST00000373477.8:c.1202C=	ENSP00000362576.4:p.Thr401=
ENST00000469100.5:n.1118C=
ENST00000478828.1:n.669C=
ENST00000487404.5:n.1512C=
ENST00000490826.1:n.495C=
NM_003680.3:c.1202C= , LRG_273t1:c.1202C=	NP_003671.1:p.Thr401=
XM_011542347.1:c.572C=	XP_011540649.1:p.Thr191=
XM_011542348.1:c.572C=	XP_011540650.1:p.Thr191=
XM_011542347.2:c.572C=	XP_011540649.1:p.Thr191=
XM_017002651.2:c.572C=	XP_016858140.1:p.Thr191=
NM_003680.4:c.1202C= MANE Select	NP_003671.1:p.Thr401=