Canonical Allele Identifier: CA2838197078
Gene: PBXIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.154946194dup , CM000663.2:g.154946194dup GRCh38
NC_000001.10:g.154918670dup , CM000663.1:g.154918670dup GRCh37
NC_000001.9:g.153185294dup NCBI36
NG_053028.1:g.1458dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368463.8:c.1481dup MANE Select ENSP00000357448.3:p.Glu495GlyfsTer?
ENST00000368463.7:c.1481dup ENSP00000357448.3:p.Glu495GlyfsTer?
ENST00000368465.5:c.1394dup ENSP00000357450.1:p.Glu466GlyfsTer?
NM_020524.2:c.1481dup NP_065385.2:p.Glu495GlyfsTer?
NM_001317734.1:c.1394dup NP_001304663.1:p.Glu466GlyfsTer?
NM_001317735.1:c.1016dup NP_001304664.1:p.Glu340GlyfsTer?
NM_020524.3:c.1481dup NP_065385.2:p.Glu495GlyfsTer?
NM_020524.4:c.1481dup MANE Select NP_065385.2:p.Glu495GlyfsTer?
NM_001317734.2:c.1394dup NP_001304663.1:p.Glu466GlyfsTer?
NM_001317735.2:c.1016dup NP_001304664.1:p.Glu340GlyfsTer?