Canonical Allele Identifier: CA2473063186

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780200C= , CM000663.2:g.32780200C=	GRCh38
NC_000001.10:g.33245801C= , CM000663.1:g.33245801C=	GRCh37
NC_000001.9:g.33018388C=	NCBI36
NG_008408.1:g.42833G= , LRG_273:g.42833G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1072G=	ENSP00000502019.1:p.Val358=
ENST00000373477.9:c.1219G= MANE Select	ENSP00000362576.4:p.Val407=
ENST00000674629.1:c.*767G=	ENSP00000502470.1:n.*767G=
ENST00000674654.1:c.*1179G=	ENSP00000501729.1:n.*1179G=
ENST00000675785.1:c.1072G=	ENSP00000502019.1:p.Val358=
ENST00000676297.1:c.*1393G=	ENSP00000501596.1:n.*1393G=
ENST00000373477.8:c.1219G=	ENSP00000362576.4:p.Val407=
ENST00000469100.5:n.1135G=
ENST00000478828.1:n.686G=
ENST00000487404.5:n.1529G=
ENST00000490826.1:n.512G=
NM_003680.3:c.1219G= , LRG_273t1:c.1219G=	NP_003671.1:p.Val407=
XM_011542347.1:c.589G=	XP_011540649.1:p.Val197=
XM_011542348.1:c.589G=	XP_011540650.1:p.Val197=
XM_011542347.2:c.589G=	XP_011540649.1:p.Val197=
XM_017002651.2:c.589G=	XP_016858140.1:p.Val197=
NM_003680.4:c.1219G= MANE Select	NP_003671.1:p.Val407=