Canonical Allele Identifier: CA339681661
Gene: YARS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32780209T>G , CM000663.2:g.32780209T>G GRCh38
NC_000001.10:g.33245810T>G , CM000663.1:g.33245810T>G GRCh37
NC_000001.9:g.33018397T>G NCBI36
NG_008408.1:g.42824A>C , LRG_273:g.42824A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000675785.2:c.1063A>C ENSP00000502019.1:p.Ser355Arg
ENST00000373477.9:c.1210A>C MANE Select ENSP00000362576.4:p.Ser404Arg
ENST00000674629.1:c.*758A>C ENSP00000502470.1:n.*758A>C
ENST00000674654.1:c.*1170A>C ENSP00000501729.1:n.*1170A>C
ENST00000675785.1:c.1063A>C ENSP00000502019.1:p.Ser355Arg
ENST00000676297.1:c.*1384A>C ENSP00000501596.1:n.*1384A>C
ENST00000373477.8:c.1210A>C ENSP00000362576.4:p.Ser404Arg
ENST00000469100.5:n.1126A>C
ENST00000478828.1:n.677A>C
ENST00000487404.5:n.1520A>C
ENST00000490826.1:n.503A>C
NM_003680.3:c.1210A>C , LRG_273t1:c.1210A>C NP_003671.1:p.Ser404Arg
XM_011542347.1:c.580A>C XP_011540649.1:p.Ser194Arg
XM_011542348.1:c.580A>C XP_011540650.1:p.Ser194Arg
XM_011542347.2:c.580A>C XP_011540649.1:p.Ser194Arg
XM_017002651.2:c.580A>C XP_016858140.1:p.Ser194Arg
NM_003680.4:c.1210A>C MANE Select NP_003671.1:p.Ser404Arg