Canonical Allele Identifier: CA339681757
Gene: YARS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32780233C>A , CM000663.2:g.32780233C>A GRCh38
NC_000001.10:g.33245834C>A , CM000663.1:g.33245834C>A GRCh37
NC_000001.9:g.33018421C>A NCBI36
NG_008408.1:g.42800G>T , LRG_273:g.42800G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000675785.2:c.1039G>T ENSP00000502019.1:p.Glu347Ter
ENST00000373477.9:c.1186G>T MANE Select ENSP00000362576.4:p.Glu396Ter
ENST00000674629.1:c.*734G>T ENSP00000502470.1:n.*734G>T
ENST00000674654.1:c.*1146G>T ENSP00000501729.1:n.*1146G>T
ENST00000675785.1:c.1039G>T ENSP00000502019.1:p.Glu347Ter
ENST00000676297.1:c.*1360G>T ENSP00000501596.1:n.*1360G>T
ENST00000373477.8:c.1186G>T ENSP00000362576.4:p.Glu396Ter
ENST00000469100.5:n.1102G>T
ENST00000478828.1:n.653G>T
ENST00000487404.5:n.1496G>T
ENST00000490826.1:n.479G>T
NM_003680.3:c.1186G>T , LRG_273t1:c.1186G>T NP_003671.1:p.Glu396Ter
XM_011542347.1:c.556G>T XP_011540649.1:p.Glu186Ter
XM_011542348.1:c.556G>T XP_011540650.1:p.Glu186Ter
XM_011542347.2:c.556G>T XP_011540649.1:p.Glu186Ter
XM_017002651.2:c.556G>T XP_016858140.1:p.Glu186Ter
NM_003680.4:c.1186G>T MANE Select NP_003671.1:p.Glu396Ter