Canonical Allele Identifier: CA339681813
Gene: YARS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32780248T>G , CM000663.2:g.32780248T>G GRCh38
NC_000001.10:g.33245849T>G , CM000663.1:g.33245849T>G GRCh37
NC_000001.9:g.33018436T>G NCBI36
NG_008408.1:g.42785A>C , LRG_273:g.42785A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000675785.2:c.1024A>C ENSP00000502019.1:p.Lys342Gln
ENST00000373477.9:c.1171A>C MANE Select ENSP00000362576.4:p.Lys391Gln
ENST00000674629.1:c.*719A>C ENSP00000502470.1:n.*719A>C
ENST00000674654.1:c.*1131A>C ENSP00000501729.1:n.*1131A>C
ENST00000675785.1:c.1024A>C ENSP00000502019.1:p.Lys342Gln
ENST00000676297.1:c.*1345A>C ENSP00000501596.1:n.*1345A>C
ENST00000373477.8:c.1171A>C ENSP00000362576.4:p.Lys391Gln
ENST00000469100.5:n.1087A>C
ENST00000478828.1:n.638A>C
ENST00000487404.5:n.1481A>C
ENST00000490826.1:n.464A>C
NM_003680.3:c.1171A>C , LRG_273t1:c.1171A>C NP_003671.1:p.Lys391Gln
XM_011542347.1:c.541A>C XP_011540649.1:p.Lys181Gln
XM_011542348.1:c.541A>C XP_011540650.1:p.Lys181Gln
XM_011542347.2:c.541A>C XP_011540649.1:p.Lys181Gln
XM_017002651.2:c.541A>C XP_016858140.1:p.Lys181Gln
NM_003680.4:c.1171A>C MANE Select NP_003671.1:p.Lys391Gln