Canonical Allele Identifier: CA1141698814

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780276G= , CM000663.2:g.32780276G=	GRCh38
NC_000001.10:g.33245877G= , CM000663.1:g.33245877G=	GRCh37
NC_000001.9:g.33018464G=	NCBI36
NG_008408.1:g.42757C= , LRG_273:g.42757C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.996C=	ENSP00000502019.1:p.His332=
ENST00000373477.9:c.1143C= MANE Select	ENSP00000362576.4:p.His381=
ENST00000674629.1:c.*691C=	ENSP00000502470.1:n.*691C=
ENST00000674654.1:c.*1103C=	ENSP00000501729.1:n.*1103C=
ENST00000675785.1:c.996C=	ENSP00000502019.1:p.His332=
ENST00000676297.1:c.*1317C=	ENSP00000501596.1:n.*1317C=
ENST00000373477.8:c.1143C=	ENSP00000362576.4:p.His381=
ENST00000469100.5:n.1059C=
ENST00000478828.1:n.610C=
ENST00000487404.5:n.1453C=
ENST00000490826.1:n.436C=
ENST00000616261.1:c.1142C=	ENSP00000484192.1:p.Thr381=
NM_003680.3:c.1143C= , LRG_273t1:c.1143C=	NP_003671.1:p.His381=
XM_011542347.1:c.513C=	XP_011540649.1:p.His171=
XM_011542348.1:c.513C=	XP_011540650.1:p.His171=
XM_011542347.2:c.513C=	XP_011540649.1:p.His171=
XM_017002651.2:c.513C=	XP_016858140.1:p.His171=
NM_003680.4:c.1143C= MANE Select	NP_003671.1:p.His381=