Canonical Allele Identifier: CA2473063198

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780230C= , CM000663.2:g.32780230C=	GRCh38
NC_000001.10:g.33245831C= , CM000663.1:g.33245831C=	GRCh37
NC_000001.9:g.33018418C=	NCBI36
NG_008408.1:g.42803G= , LRG_273:g.42803G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1042G=	ENSP00000502019.1:p.Ala348=
ENST00000373477.9:c.1189G= MANE Select	ENSP00000362576.4:p.Ala397=
ENST00000674629.1:c.*737G=	ENSP00000502470.1:n.*737G=
ENST00000674654.1:c.*1149G=	ENSP00000501729.1:n.*1149G=
ENST00000675785.1:c.1042G=	ENSP00000502019.1:p.Ala348=
ENST00000676297.1:c.*1363G=	ENSP00000501596.1:n.*1363G=
ENST00000373477.8:c.1189G=	ENSP00000362576.4:p.Ala397=
ENST00000469100.5:n.1105G=
ENST00000478828.1:n.656G=
ENST00000487404.5:n.1499G=
ENST00000490826.1:n.482G=
NM_003680.3:c.1189G= , LRG_273t1:c.1189G=	NP_003671.1:p.Ala397=
XM_011542347.1:c.559G=	XP_011540649.1:p.Ala187=
XM_011542348.1:c.559G=	XP_011540650.1:p.Ala187=
XM_011542347.2:c.559G=	XP_011540649.1:p.Ala187=
XM_017002651.2:c.559G=	XP_016858140.1:p.Ala187=
NM_003680.4:c.1189G= MANE Select	NP_003671.1:p.Ala397=