Canonical Allele Identifier: CA2473076934

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32811146C= , CM000663.2:g.32811146C=	GRCh38
NC_000001.10:g.33276747C= , CM000663.1:g.33276747C=	GRCh37
NC_000001.9:g.33049334C=	NCBI36
NG_008408.1:g.11887G= , LRG_273:g.11887G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.58-380G=	ENSP00000502019.1:n.58-380G=
ENST00000373477.9:c.58-89G= MANE Select	ENSP00000362576.4:n.58-89G=
ENST00000481895.6:c.58-89G=	ENSP00000502016.1:n.58-89G=
ENST00000616261.2:c.58-89G=	ENSP00000484192.2:n.58-89G=
ENST00000674629.1:c.58-4535G=	ENSP00000502470.1:n.58-4535G=
ENST00000674654.1:c.58-89G=	ENSP00000501729.1:n.58-89G=
ENST00000675785.1:c.58-380G=	ENSP00000502019.1:n.58-380G=
ENST00000676297.1:c.58-89G=	ENSP00000501596.1:n.58-89G=
ENST00000373477.8:c.58-89G=	ENSP00000362576.4:n.58-89G=
ENST00000472692.1:n.502G=
ENST00000481895.5:n.131-89G=
ENST00000616261.1:c.58-89G=	ENSP00000484192.1:n.58-89G=
NM_003680.3:c.58-89G= , LRG_273t1:c.58-89G=	NP_003671.1:n.58-89G=
XM_011542347.1:c.-250-4535G=	XP_011540649.1:n.-250-4535G=
XM_011542348.1:c.-297-4535G=	XP_011540650.1:n.-297-4535G=
XM_011542347.2:c.-250-4535G=	XP_011540649.1:n.-250-4535G=
XM_017002651.2:c.-620-89G=	XP_016858140.1:n.-620-89G=
NM_003680.4:c.58-89G= MANE Select	NP_003671.1:n.58-89G=