Canonical Allele Identifier: CA1140587467

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32782412G= , CM000663.2:g.32782412G=	GRCh38
NC_000001.10:g.33248013G= , CM000663.1:g.33248013G=	GRCh37
NC_000001.9:g.33020600G=	NCBI36
NG_008408.1:g.40621C= , LRG_273:g.40621C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000675785.2:c.887C=	ENSP00000502019.1:p.Ser296=
ENST00000373477.9:c.1034C= MANE Select	ENSP00000362576.4:p.Ser345=
ENST00000674629.1:c.*582C=	ENSP00000502470.1:n.*582C=
ENST00000674654.1:c.*994C=	ENSP00000501729.1:n.*994C=
ENST00000675785.1:c.887C=	ENSP00000502019.1:p.Ser296=
ENST00000676297.1:c.*1208C=	ENSP00000501596.1:n.*1208C=
ENST00000373477.8:c.1034C=	ENSP00000362576.4:p.Ser345=
ENST00000478828.1:n.501C=
ENST00000487404.5:n.1344C=
ENST00000616261.1:c.1034C=	ENSP00000484192.1:p.Ser345=
NM_003680.3:c.1034C= , LRG_273t1:c.1034C=	NP_003671.1:p.Ser345=
XM_011542347.1:c.404C=	XP_011540649.1:p.Ser135=
XM_011542348.1:c.404C=	XP_011540650.1:p.Ser135=
XM_011542347.2:c.404C=	XP_011540649.1:p.Ser135=
XM_017002651.2:c.404C=	XP_016858140.1:p.Ser135=
NM_003680.4:c.1034C= MANE Select	NP_003671.1:p.Ser345=