Canonical Allele Identifier: CA2473063190

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780214A= , CM000663.2:g.32780214A=	GRCh38
NC_000001.10:g.33245815A= , CM000663.1:g.33245815A=	GRCh37
NC_000001.9:g.33018402A=	NCBI36
NG_008408.1:g.42819T= , LRG_273:g.42819T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1058T=	ENSP00000502019.1:p.Val353=
ENST00000373477.9:c.1205T= MANE Select	ENSP00000362576.4:p.Val402=
ENST00000674629.1:c.*753T=	ENSP00000502470.1:n.*753T=
ENST00000674654.1:c.*1165T=	ENSP00000501729.1:n.*1165T=
ENST00000675785.1:c.1058T=	ENSP00000502019.1:p.Val353=
ENST00000676297.1:c.*1379T=	ENSP00000501596.1:n.*1379T=
ENST00000373477.8:c.1205T=	ENSP00000362576.4:p.Val402=
ENST00000469100.5:n.1121T=
ENST00000478828.1:n.672T=
ENST00000487404.5:n.1515T=
ENST00000490826.1:n.498T=
NM_003680.3:c.1205T= , LRG_273t1:c.1205T=	NP_003671.1:p.Val402=
XM_011542347.1:c.575T=	XP_011540649.1:p.Val192=
XM_011542348.1:c.575T=	XP_011540650.1:p.Val192=
XM_011542347.2:c.575T=	XP_011540649.1:p.Val192=
XM_017002651.2:c.575T=	XP_016858140.1:p.Val192=
NM_003680.4:c.1205T= MANE Select	NP_003671.1:p.Val402=