Canonical Allele Identifier: CA2473063206
Gene: YARS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.32780265T= , CM000663.2:g.32780265T= GRCh38
NC_000001.10:g.33245866T= , CM000663.1:g.33245866T= GRCh37
NC_000001.9:g.33018453T= NCBI36
NG_008408.1:g.42768A= , LRG_273:g.42768A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000675785.2:c.1007A= ENSP00000502019.1:p.Asp336=
ENST00000373477.9:c.1154A= MANE Select ENSP00000362576.4:p.Asp385=
ENST00000674629.1:c.*702A= ENSP00000502470.1:n.*702A=
ENST00000674654.1:c.*1114A= ENSP00000501729.1:n.*1114A=
ENST00000675785.1:c.1007A= ENSP00000502019.1:p.Asp336=
ENST00000676297.1:c.*1328A= ENSP00000501596.1:n.*1328A=
ENST00000373477.8:c.1154A= ENSP00000362576.4:p.Asp385=
ENST00000469100.5:n.1070A=
ENST00000478828.1:n.621A=
ENST00000487404.5:n.1464A=
ENST00000490826.1:n.447A=
ENST00000616261.1:c.1153A= ENSP00000484192.1:p.Thr385=
NM_003680.3:c.1154A= , LRG_273t1:c.1154A= NP_003671.1:p.Asp385=
XM_011542347.1:c.524A= XP_011540649.1:p.Asp175=
XM_011542348.1:c.524A= XP_011540650.1:p.Asp175=
XM_011542347.2:c.524A= XP_011540649.1:p.Asp175=
XM_017002651.2:c.524A= XP_016858140.1:p.Asp175=
NM_003680.4:c.1154A= MANE Select NP_003671.1:p.Asp385=