Canonical Allele Identifier: CA2026286173
Gene: YARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32755501C= , CM000674.2:g.32755501C= GRCh38
NC_000012.11:g.32908435C= , CM000674.1:g.32908435C= GRCh37
NC_000012.10:g.32799702C= NCBI36
NG_028122.1:g.5453G=

Transcript Alleles

HGVS Amino-acid Change
NM_001040436.3:c.374G= MANE Select NP_001035526.1:p.Arg125=
ENST00000324868.13:c.374G= MANE Select ENSP00000320658.8:p.Arg125=
NM_001040436.2:c.374G= NP_001035526.1:p.Arg125=
ENST00000324868.12:c.374G= ENSP00000320658.8:p.Arg125=
ENST00000548490.1:c.296G= ENSP00000447710.1:p.Arg99=
XR_001748730.2:n.958G=
XR_002957331.1:n.958G=
XR_242891.3:n.461G=
XR_242892.3:n.461G=
XR_242892.5:n.958G=
XR_429036.1:n.461G=
XR_931296.1:n.461G=
XR_931296.3:n.958G=
XR_931297.1:n.461G=
XR_931298.1:n.461G=
XR_931299.1:n.461G=