Canonical Allele Identifier: CA192954049
Community Standard Title: NM_016042.4(EXOSC3):c.151C>T (p.Arg51Ter)
Gene: EXOSC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37784894G>A , CM000671.2:g.37784894G>A GRCh38
NC_000009.11:g.37784891G>A , CM000671.1:g.37784891G>A GRCh37
NC_000009.10:g.37774891G>A NCBI36
NG_032780.1:g.5199C>T

Transcript Alleles

HGVS Amino-acid Change
NM_016042.4:c.151C>T MANE Select NP_057126.2:p.Arg51Ter
ENST00000327304.10:c.151C>T MANE Select ENSP00000323046.4:p.Arg51Ter
NM_001002269.2:c.151C>T NP_001002269.1:p.Arg51Ter
NM_016042.3:c.151C>T NP_057126.2:p.Arg51Ter
ENST00000327304.9:c.151C>T ENSP00000323046.4:p.Arg51Ter
ENST00000396521.3:c.151C>T ENSP00000379775.3:p.Arg51Ter
ENST00000465229.5:c.151C>T ENSP00000418422.1:p.Arg51Ter
ENST00000482614.5:n.86-831C>T
ENST00000489414.5:n.44-831C>T
ENST00000540557.1:c.*761-831C>T ENSP00000457548.1:n.*761-831C>T
ENST00000678095.1:c.-70-831C>T ENSP00000503205.1:n.-70-831C>T
ENST00000678588.1:n.171C>T
ENST00000679059.1:c.151C>T ENSP00000503947.1:p.Arg51Ter