Canonical Allele Identifier: CA1143494208

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780294G= , CM000663.2:g.32780294G=	GRCh38
NC_000001.10:g.33245895G= , CM000663.1:g.33245895G=	GRCh37
NC_000001.9:g.33018482G=	NCBI36
NG_008408.1:g.42739C= , LRG_273:g.42739C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.994-16C=	ENSP00000502019.1:n.994-16C=
ENST00000373477.9:c.1141-16C= MANE Select	ENSP00000362576.4:n.1141-16C=
ENST00000674629.1:c.*689-16C=	ENSP00000502470.1:n.*689-16C=
ENST00000674654.1:c.*1101-16C=	ENSP00000501729.1:n.*1101-16C=
ENST00000675785.1:c.994-16C=	ENSP00000502019.1:n.994-16C=
ENST00000676297.1:c.*1315-16C=	ENSP00000501596.1:n.*1315-16C=
ENST00000373477.8:c.1141-16C=	ENSP00000362576.4:n.1141-16C=
ENST00000469100.5:n.1057-16C=
ENST00000478828.1:n.608-16C=
ENST00000487404.5:n.1451-16C=
ENST00000490826.1:n.418C=
ENST00000616261.1:c.1140-16C=	ENSP00000484192.1:n.1140-16C=
NM_003680.3:c.1141-16C= , LRG_273t1:c.1141-16C=	NP_003671.1:n.1141-16C=
XM_011542347.1:c.511-16C=	XP_011540649.1:n.511-16C=
XM_011542348.1:c.511-16C=	XP_011540650.1:n.511-16C=
XM_011542347.2:c.511-16C=	XP_011540649.1:n.511-16C=
XM_017002651.2:c.511-16C=	XP_016858140.1:n.511-16C=
NM_003680.4:c.1141-16C= MANE Select	NP_003671.1:n.1141-16C=