Canonical Allele Identifier: CA339681875
Gene: YARS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32780262C>G , CM000663.2:g.32780262C>G GRCh38
NC_000001.10:g.33245863C>G , CM000663.1:g.33245863C>G GRCh37
NC_000001.9:g.33018450C>G NCBI36
NG_008408.1:g.42771G>C , LRG_273:g.42771G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000675785.2:c.1010G>C ENSP00000502019.1:p.Ser337Thr
ENST00000373477.9:c.1157G>C MANE Select ENSP00000362576.4:p.Ser386Thr
ENST00000674629.1:c.*705G>C ENSP00000502470.1:n.*705G>C
ENST00000674654.1:c.*1117G>C ENSP00000501729.1:n.*1117G>C
ENST00000675785.1:c.1010G>C ENSP00000502019.1:p.Ser337Thr
ENST00000676297.1:c.*1331G>C ENSP00000501596.1:n.*1331G>C
ENST00000373477.8:c.1157G>C ENSP00000362576.4:p.Ser386Thr
ENST00000469100.5:n.1073G>C
ENST00000478828.1:n.624G>C
ENST00000487404.5:n.1467G>C
ENST00000490826.1:n.450G>C
ENST00000616261.1:c.1156G>C ENSP00000484192.1:p.Ala386Pro
NM_003680.3:c.1157G>C , LRG_273t1:c.1157G>C NP_003671.1:p.Ser386Thr
XM_011542347.1:c.527G>C XP_011540649.1:p.Ser176Thr
XM_011542348.1:c.527G>C XP_011540650.1:p.Ser176Thr
XM_011542347.2:c.527G>C XP_011540649.1:p.Ser176Thr
XM_017002651.2:c.527G>C XP_016858140.1:p.Ser176Thr
NM_003680.4:c.1157G>C MANE Select NP_003671.1:p.Ser386Thr