Canonical Allele Identifier: CA1149114633

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780244A= , CM000663.2:g.32780244A=	GRCh38
NC_000001.10:g.33245845A= , CM000663.1:g.33245845A=	GRCh37
NC_000001.9:g.33018432A=	NCBI36
NG_008408.1:g.42789T= , LRG_273:g.42789T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1028T=	ENSP00000502019.1:p.Ile343=
ENST00000373477.9:c.1175T= MANE Select	ENSP00000362576.4:p.Ile392=
ENST00000674629.1:c.*723T=	ENSP00000502470.1:n.*723T=
ENST00000674654.1:c.*1135T=	ENSP00000501729.1:n.*1135T=
ENST00000675785.1:c.1028T=	ENSP00000502019.1:p.Ile343=
ENST00000676297.1:c.*1349T=	ENSP00000501596.1:n.*1349T=
ENST00000373477.8:c.1175T=	ENSP00000362576.4:p.Ile392=
ENST00000469100.5:n.1091T=
ENST00000478828.1:n.642T=
ENST00000487404.5:n.1485T=
ENST00000490826.1:n.468T=
NM_003680.3:c.1175T= , LRG_273t1:c.1175T=	NP_003671.1:p.Ile392=
XM_011542347.1:c.545T=	XP_011540649.1:p.Ile182=
XM_011542348.1:c.545T=	XP_011540650.1:p.Ile182=
XM_011542347.2:c.545T=	XP_011540649.1:p.Ile182=
XM_017002651.2:c.545T=	XP_016858140.1:p.Ile182=
NM_003680.4:c.1175T= MANE Select	NP_003671.1:p.Ile392=