Canonical Allele Identifier: CA2473063181

Gene: YARS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32780185T= , CM000663.2:g.32780185T=	GRCh38
NC_000001.10:g.33245786T= , CM000663.1:g.33245786T=	GRCh37
NC_000001.9:g.33018373T=	NCBI36
NG_008408.1:g.42848A= , LRG_273:g.42848A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000675785.2:c.1087A=	ENSP00000502019.1:p.Lys363=
ENST00000373477.9:c.1234A= MANE Select	ENSP00000362576.4:p.Lys412=
ENST00000674629.1:c.*782A=	ENSP00000502470.1:n.*782A=
ENST00000674654.1:c.*1194A=	ENSP00000501729.1:n.*1194A=
ENST00000675785.1:c.1087A=	ENSP00000502019.1:p.Lys363=
ENST00000676297.1:c.*1408A=	ENSP00000501596.1:n.*1408A=
ENST00000373477.8:c.1234A=	ENSP00000362576.4:p.Lys412=
ENST00000469100.5:n.1150A=
ENST00000478828.1:n.701A=
ENST00000487404.5:n.1544A=
ENST00000490826.1:n.527A=
NM_003680.3:c.1234A= , LRG_273t1:c.1234A=	NP_003671.1:p.Lys412=
XM_011542347.1:c.604A=	XP_011540649.1:p.Lys202=
XM_011542348.1:c.604A=	XP_011540650.1:p.Lys202=
XM_011542347.2:c.604A=	XP_011540649.1:p.Lys202=
XM_017002651.2:c.604A=	XP_016858140.1:p.Lys202=
NM_003680.4:c.1234A= MANE Select	NP_003671.1:p.Lys412=