Canonical Allele Identifier: CA1139824895

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780201C= , CM000663.2:g.32780201C=	GRCh38
NC_000001.10:g.33245802C= , CM000663.1:g.33245802C=	GRCh37
NC_000001.9:g.33018389C=	NCBI36
NG_008408.1:g.42832G= , LRG_273:g.42832G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1071G=	ENSP00000502019.1:p.Leu357=
ENST00000373477.9:c.1218G= MANE Select	ENSP00000362576.4:p.Leu406=
ENST00000674629.1:c.*766G=	ENSP00000502470.1:n.*766G=
ENST00000674654.1:c.*1178G=	ENSP00000501729.1:n.*1178G=
ENST00000675785.1:c.1071G=	ENSP00000502019.1:p.Leu357=
ENST00000676297.1:c.*1392G=	ENSP00000501596.1:n.*1392G=
ENST00000373477.8:c.1218G=	ENSP00000362576.4:p.Leu406=
ENST00000469100.5:n.1134G=
ENST00000478828.1:n.685G=
ENST00000487404.5:n.1528G=
ENST00000490826.1:n.511G=
NM_003680.3:c.1218G= , LRG_273t1:c.1218G=	NP_003671.1:p.Leu406=
XM_011542347.1:c.588G=	XP_011540649.1:p.Leu196=
XM_011542348.1:c.588G=	XP_011540650.1:p.Leu196=
XM_011542347.2:c.588G=	XP_011540649.1:p.Leu196=
XM_017002651.2:c.588G=	XP_016858140.1:p.Leu196=
NM_003680.4:c.1218G= MANE Select	NP_003671.1:p.Leu406=