Canonical Allele Identifier: CA2473063177
Gene: YARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32780174C= , CM000663.2:g.32780174C= GRCh38
NC_000001.10:g.33245775C= , CM000663.1:g.33245775C= GRCh37
NC_000001.9:g.33018362C= NCBI36
NG_008408.1:g.42859G= , LRG_273:g.42859G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000675785.2:c.1098G= ENSP00000502019.1:p.Leu366=
ENST00000373477.9:c.1245G= MANE Select ENSP00000362576.4:p.Leu415=
ENST00000674629.1:c.*793G= ENSP00000502470.1:n.*793G=
ENST00000674654.1:c.*1205G= ENSP00000501729.1:n.*1205G=
ENST00000675785.1:c.1098G= ENSP00000502019.1:p.Leu366=
ENST00000676297.1:c.*1419G= ENSP00000501596.1:n.*1419G=
ENST00000373477.8:c.1245G= ENSP00000362576.4:p.Leu415=
ENST00000469100.5:n.1161G=
ENST00000478828.1:n.712G=
ENST00000487404.5:n.1555G=
ENST00000490826.1:n.538G=
NM_003680.3:c.1245G= , LRG_273t1:c.1245G= NP_003671.1:p.Leu415=
XM_011542347.1:c.615G= XP_011540649.1:p.Leu205=
XM_011542348.1:c.615G= XP_011540650.1:p.Leu205=
XM_011542347.2:c.615G= XP_011540649.1:p.Leu205=
XM_017002651.2:c.615G= XP_016858140.1:p.Leu205=
NM_003680.4:c.1245G= MANE Select NP_003671.1:p.Leu415=