Canonical Allele Identifier: CA339681822
Gene: YARS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32780251C>A , CM000663.2:g.32780251C>A GRCh38
NC_000001.10:g.33245852C>A , CM000663.1:g.33245852C>A GRCh37
NC_000001.9:g.33018439C>A NCBI36
NG_008408.1:g.42782G>T , LRG_273:g.42782G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000675785.2:c.1021G>T ENSP00000502019.1:p.Glu341Ter
ENST00000373477.9:c.1168G>T MANE Select ENSP00000362576.4:p.Glu390Ter
ENST00000674629.1:c.*716G>T ENSP00000502470.1:n.*716G>T
ENST00000674654.1:c.*1128G>T ENSP00000501729.1:n.*1128G>T
ENST00000675785.1:c.1021G>T ENSP00000502019.1:p.Glu341Ter
ENST00000676297.1:c.*1342G>T ENSP00000501596.1:n.*1342G>T
ENST00000373477.8:c.1168G>T ENSP00000362576.4:p.Glu390Ter
ENST00000469100.5:n.1084G>T
ENST00000478828.1:n.635G>T
ENST00000487404.5:n.1478G>T
ENST00000490826.1:n.461G>T
ENST00000616261.1:c.1167G>T ENSP00000484192.1:p.Ter389Tyr
NM_003680.3:c.1168G>T , LRG_273t1:c.1168G>T NP_003671.1:p.Glu390Ter
XM_011542347.1:c.538G>T XP_011540649.1:p.Glu180Ter
XM_011542348.1:c.538G>T XP_011540650.1:p.Glu180Ter
XM_011542347.2:c.538G>T XP_011540649.1:p.Glu180Ter
XM_017002651.2:c.538G>T XP_016858140.1:p.Glu180Ter
NM_003680.4:c.1168G>T MANE Select NP_003671.1:p.Glu390Ter