Canonical Allele Identifier: CA1777236941
Gene: PLPBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37765752T= , CM000670.2:g.37765752T= GRCh38
NC_000008.10:g.37623270T= , CM000670.1:g.37623270T= GRCh37
NC_000008.9:g.37742428T= NCBI36
NG_053030.1:g.9000T=

Transcript Alleles

HGVS Amino-acid change
ENST00000328195.8:c.243+6T= MANE Select ENSP00000333551.3:n.243+6T=
ENST00000328195.7:c.243+6T= ENSP00000333551.3:n.243+6T=
ENST00000518036.5:c.*95+6T= ENSP00000428005.1:n.*95+6T=
ENST00000520073.5:n.308+6T=
ENST00000523187.5:c.87+6T= ENSP00000427886.1:n.87+6T=
ENST00000523358.5:c.243+6T= ENSP00000427778.1:n.243+6T=
ENST00000523994.1:n.248+6T=
NM_007198.3:c.243+6T= NP_009129.1:n.243+6T=
NM_001349346.1:c.243+6T= NP_001336275.1:n.243+6T=
NM_001349347.1:c.237+6T= NP_001336276.1:n.237+6T=
NM_001349348.1:c.87+6T= NP_001336277.1:n.87+6T=
NM_001349349.1:c.348+6T= NP_001336278.1:n.348+6T=
NM_007198.4:c.243+6T= MANE Select NP_009129.1:n.243+6T=
NM_001349346.2:c.243+6T= NP_001336275.1:n.243+6T=
NM_001349347.2:c.237+6T= NP_001336276.1:n.237+6T=
NM_001349348.2:c.87+6T= NP_001336277.1:n.87+6T=