Canonical Allele Identifier: CA339681310
Gene: YARS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32780128T>G , CM000663.2:g.32780128T>G GRCh38
NC_000001.10:g.33245729T>G , CM000663.1:g.33245729T>G GRCh37
NC_000001.9:g.33018316T>G NCBI36
NG_008408.1:g.42905A>C , LRG_273:g.42905A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000675785.2:c.1144A>C ENSP00000502019.1:p.Met382Leu
ENST00000373477.9:c.1291A>C MANE Select ENSP00000362576.4:p.Met431Leu
ENST00000674629.1:c.*839A>C ENSP00000502470.1:n.*839A>C
ENST00000674654.1:c.*1251A>C ENSP00000501729.1:n.*1251A>C
ENST00000675785.1:c.1144A>C ENSP00000502019.1:p.Met382Leu
ENST00000676297.1:c.*1465A>C ENSP00000501596.1:n.*1465A>C
ENST00000373477.8:c.1291A>C ENSP00000362576.4:p.Met431Leu
ENST00000469100.5:n.1207A>C
ENST00000478828.1:n.758A>C
ENST00000487404.5:n.1601A>C
ENST00000490826.1:n.584A>C
NM_003680.3:c.1291A>C , LRG_273t1:c.1291A>C NP_003671.1:p.Met431Leu
XM_011542347.1:c.661A>C XP_011540649.1:p.Met221Leu
XM_011542348.1:c.661A>C XP_011540650.1:p.Met221Leu
XM_011542347.2:c.661A>C XP_011540649.1:p.Met221Leu
XM_017002651.2:c.661A>C XP_016858140.1:p.Met221Leu
NM_003680.4:c.1291A>C MANE Select NP_003671.1:p.Met431Leu