Canonical Allele Identifier: CA2473076943

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32811168C= , CM000663.2:g.32811168C=	GRCh38
NC_000001.10:g.33276769C= , CM000663.1:g.33276769C=	GRCh37
NC_000001.9:g.33049356C=	NCBI36
NG_008408.1:g.11865G= , LRG_273:g.11865G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.58-402G=	ENSP00000502019.1:n.58-402G=
ENST00000373477.9:c.58-111G= MANE Select	ENSP00000362576.4:n.58-111G=
ENST00000481895.6:c.58-111G=	ENSP00000502016.1:n.58-111G=
ENST00000616261.2:c.58-111G=	ENSP00000484192.2:n.58-111G=
ENST00000674629.1:c.58-4557G=	ENSP00000502470.1:n.58-4557G=
ENST00000674654.1:c.58-111G=	ENSP00000501729.1:n.58-111G=
ENST00000675785.1:c.58-402G=	ENSP00000502019.1:n.58-402G=
ENST00000676297.1:c.58-111G=	ENSP00000501596.1:n.58-111G=
ENST00000373477.8:c.58-111G=	ENSP00000362576.4:n.58-111G=
ENST00000472692.1:n.480G=
ENST00000481895.5:n.131-111G=
ENST00000616261.1:c.58-111G=	ENSP00000484192.1:n.58-111G=
NM_003680.3:c.58-111G= , LRG_273t1:c.58-111G=	NP_003671.1:n.58-111G=
XM_011542347.1:c.-250-4557G=	XP_011540649.1:n.-250-4557G=
XM_011542348.1:c.-297-4557G=	XP_011540650.1:n.-297-4557G=
XM_011542347.2:c.-250-4557G=	XP_011540649.1:n.-250-4557G=
XM_017002651.2:c.-620-111G=	XP_016858140.1:n.-620-111G=
NM_003680.4:c.58-111G= MANE Select	NP_003671.1:n.58-111G=