Canonical Allele Identifier: CA2026283379
Gene: YARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.32753932G= , CM000674.2:g.32753932G= GRCh38
NC_000012.11:g.32906866G= , CM000674.1:g.32906866G= GRCh37
NC_000012.10:g.32798133G= NCBI36
NG_028122.1:g.7022C=

Transcript Alleles

HGVS Amino-acid Change
NM_001040436.3:c.933C= MANE Select NP_001035526.1:p.Asp311=
ENST00000324868.13:c.933C= MANE Select ENSP00000320658.8:p.Asp311=
NM_001040436.2:c.933C= NP_001035526.1:p.Asp311=
ENST00000324868.12:c.933C= ENSP00000320658.8:p.Asp311=
ENST00000548490.1:c.855C= ENSP00000447710.1:p.Asp285=
XR_001748730.2:n.1517C=
XR_002957331.1:n.1517C=
XR_242891.3:n.1020C=
XR_242892.3:n.1020C=
XR_242892.5:n.1517C=
XR_429036.1:n.1020C=
XR_931296.1:n.1020C=
XR_931296.3:n.1517C=
XR_931297.1:n.1020C=
XR_931298.1:n.1020C=
XR_931299.1:n.1020C=