Canonical Allele Identifier: CA2473063234
Gene: YARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32780336G= , CM000663.2:g.32780336G= GRCh38
NC_000001.10:g.33245937G= , CM000663.1:g.33245937G= GRCh37
NC_000001.9:g.33018524G= NCBI36
NG_008408.1:g.42697C= , LRG_273:g.42697C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000675785.2:c.994-58C= ENSP00000502019.1:n.994-58C=
ENST00000373477.9:c.1141-58C= MANE Select ENSP00000362576.4:n.1141-58C=
ENST00000674629.1:c.*689-58C= ENSP00000502470.1:n.*689-58C=
ENST00000674654.1:c.*1101-58C= ENSP00000501729.1:n.*1101-58C=
ENST00000675785.1:c.994-58C= ENSP00000502019.1:n.994-58C=
ENST00000676297.1:c.*1315-58C= ENSP00000501596.1:n.*1315-58C=
ENST00000373477.8:c.1141-58C= ENSP00000362576.4:n.1141-58C=
ENST00000469100.5:n.1057-58C=
ENST00000478828.1:n.608-58C=
ENST00000487404.5:n.1451-58C=
ENST00000490826.1:n.376C=
ENST00000616261.1:c.1140-58C= ENSP00000484192.1:n.1140-58C=
NM_003680.3:c.1141-58C= , LRG_273t1:c.1141-58C= NP_003671.1:n.1141-58C=
XM_011542347.1:c.511-58C= XP_011540649.1:n.511-58C=
XM_011542348.1:c.511-58C= XP_011540650.1:n.511-58C=
XM_011542347.2:c.511-58C= XP_011540649.1:n.511-58C=
XM_017002651.2:c.511-58C= XP_016858140.1:n.511-58C=
NM_003680.4:c.1141-58C= MANE Select NP_003671.1:n.1141-58C=