Canonical Allele Identifier: CA1143049257

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780195C= , CM000663.2:g.32780195C=	GRCh38
NC_000001.10:g.33245796C= , CM000663.1:g.33245796C=	GRCh37
NC_000001.9:g.33018383C=	NCBI36
NG_008408.1:g.42838G= , LRG_273:g.42838G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1077G=	ENSP00000502019.1:p.Gln359=
ENST00000373477.9:c.1224G= MANE Select	ENSP00000362576.4:p.Gln408=
ENST00000674629.1:c.*772G=	ENSP00000502470.1:n.*772G=
ENST00000674654.1:c.*1184G=	ENSP00000501729.1:n.*1184G=
ENST00000675785.1:c.1077G=	ENSP00000502019.1:p.Gln359=
ENST00000676297.1:c.*1398G=	ENSP00000501596.1:n.*1398G=
ENST00000373477.8:c.1224G=	ENSP00000362576.4:p.Gln408=
ENST00000469100.5:n.1140G=
ENST00000478828.1:n.691G=
ENST00000487404.5:n.1534G=
ENST00000490826.1:n.517G=
NM_003680.3:c.1224G= , LRG_273t1:c.1224G=	NP_003671.1:p.Gln408=
XM_011542347.1:c.594G=	XP_011540649.1:p.Gln198=
XM_011542348.1:c.594G=	XP_011540650.1:p.Gln198=
XM_011542347.2:c.594G=	XP_011540649.1:p.Gln198=
XM_017002651.2:c.594G=	XP_016858140.1:p.Gln198=
NM_003680.4:c.1224G= MANE Select	NP_003671.1:p.Gln408=