Canonical Allele Identifier: CA1144043737

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780215C= , CM000663.2:g.32780215C=	GRCh38
NC_000001.10:g.33245816C= , CM000663.1:g.33245816C=	GRCh37
NC_000001.9:g.33018403C=	NCBI36
NG_008408.1:g.42818G= , LRG_273:g.42818G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1057G=	ENSP00000502019.1:p.Val353=
ENST00000373477.9:c.1204G= MANE Select	ENSP00000362576.4:p.Val402=
ENST00000674629.1:c.*752G=	ENSP00000502470.1:n.*752G=
ENST00000674654.1:c.*1164G=	ENSP00000501729.1:n.*1164G=
ENST00000675785.1:c.1057G=	ENSP00000502019.1:p.Val353=
ENST00000676297.1:c.*1378G=	ENSP00000501596.1:n.*1378G=
ENST00000373477.8:c.1204G=	ENSP00000362576.4:p.Val402=
ENST00000469100.5:n.1120G=
ENST00000478828.1:n.671G=
ENST00000487404.5:n.1514G=
ENST00000490826.1:n.497G=
NM_003680.3:c.1204G= , LRG_273t1:c.1204G=	NP_003671.1:p.Val402=
XM_011542347.1:c.574G=	XP_011540649.1:p.Val192=
XM_011542348.1:c.574G=	XP_011540650.1:p.Val192=
XM_011542347.2:c.574G=	XP_011540649.1:p.Val192=
XM_017002651.2:c.574G=	XP_016858140.1:p.Val192=
NM_003680.4:c.1204G= MANE Select	NP_003671.1:p.Val402=