Canonical Allele Identifier: CA417063598
Gene: YARS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.33245688A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32780087A>T , CM000663.2:g.32780087A>T GRCh38
NC_000001.10:g.33245688A>T , CM000663.1:g.33245688A>T GRCh37
NC_000001.9:g.33018275A>T NCBI36
NG_008408.1:g.42946T>A , LRG_273:g.42946T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000675785.2:c.1185T>A ENSP00000502019.1:p.Ser395=
ENST00000373477.9:c.1332T>A MANE Select ENSP00000362576.4:p.Ser444=
ENST00000674629.1:c.*880T>A ENSP00000502470.1:n.*880T>A
ENST00000674654.1:c.*1292T>A ENSP00000501729.1:n.*1292T>A
ENST00000675785.1:c.1185T>A ENSP00000502019.1:p.Ser395=
ENST00000676297.1:c.*1506T>A ENSP00000501596.1:n.*1506T>A
ENST00000373477.8:c.1332T>A ENSP00000362576.4:p.Ser444=
ENST00000469100.5:n.1248T>A
ENST00000478828.1:n.799T>A
ENST00000487404.5:n.1642T>A
ENST00000490826.1:n.625T>A
NM_003680.3:c.1332T>A , LRG_273t1:c.1332T>A NP_003671.1:p.Ser444=
XM_011542347.1:c.702T>A XP_011540649.1:p.Ser234=
XM_011542348.1:c.702T>A XP_011540650.1:p.Ser234=
XM_011542347.2:c.702T>A XP_011540649.1:p.Ser234=
XM_017002651.2:c.702T>A XP_016858140.1:p.Ser234=
NM_003680.4:c.1332T>A MANE Select NP_003671.1:p.Ser444=