Canonical Allele Identifier: CA1141001758

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780173G= , CM000663.2:g.32780173G=	GRCh38
NC_000001.10:g.33245774G= , CM000663.1:g.33245774G=	GRCh37
NC_000001.9:g.33018361G=	NCBI36
NG_008408.1:g.42860C= , LRG_273:g.42860C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1099C=	ENSP00000502019.1:p.Gln367=
ENST00000373477.9:c.1246C= MANE Select	ENSP00000362576.4:p.Gln416=
ENST00000674629.1:c.*794C=	ENSP00000502470.1:n.*794C=
ENST00000674654.1:c.*1206C=	ENSP00000501729.1:n.*1206C=
ENST00000675785.1:c.1099C=	ENSP00000502019.1:p.Gln367=
ENST00000676297.1:c.*1420C=	ENSP00000501596.1:n.*1420C=
ENST00000373477.8:c.1246C=	ENSP00000362576.4:p.Gln416=
ENST00000469100.5:n.1162C=
ENST00000478828.1:n.713C=
ENST00000487404.5:n.1556C=
ENST00000490826.1:n.539C=
NM_003680.3:c.1246C= , LRG_273t1:c.1246C=	NP_003671.1:p.Gln416=
XM_011542347.1:c.616C=	XP_011540649.1:p.Gln206=
XM_011542348.1:c.616C=	XP_011540650.1:p.Gln206=
XM_011542347.2:c.616C=	XP_011540649.1:p.Gln206=
XM_017002651.2:c.616C=	XP_016858140.1:p.Gln206=
NM_003680.4:c.1246C= MANE Select	NP_003671.1:p.Gln416=