Canonical Allele Identifier: CA1777236803
Gene: PLPBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37765445A= , CM000670.2:g.37765445A= GRCh38
NC_000008.10:g.37622963A= , CM000670.1:g.37622963A= GRCh37
NC_000008.9:g.37742121A= NCBI36
NG_053030.1:g.8693A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328195.8:c.100-81A= MANE Select ENSP00000333551.3:n.100-81A=
ENST00000328195.7:c.100-81A= ENSP00000333551.3:n.100-81A=
ENST00000518036.5:c.100-81A= ENSP00000428005.1:n.100-81A=
ENST00000520073.5:n.165-81A=
ENST00000523187.5:c.-57-81A= ENSP00000427886.1:n.-57-81A=
ENST00000523358.5:c.100-81A= ENSP00000427778.1:n.100-81A=
ENST00000523994.1:n.105-81A=
NM_007198.3:c.100-81A= NP_009129.1:n.100-81A=
NM_001349346.1:c.100-81A= NP_001336275.1:n.100-81A=
NM_001349347.1:c.100-81A= NP_001336276.1:n.100-81A=
NM_001349348.1:c.-57-81A= NP_001336277.1:n.-57-81A=
NM_001349349.1:c.205-81A= NP_001336278.1:n.205-81A=
NM_007198.4:c.100-81A= MANE Select NP_009129.1:n.100-81A=
NM_001349346.2:c.100-81A= NP_001336275.1:n.100-81A=
NM_001349347.2:c.100-81A= NP_001336276.1:n.100-81A=
NM_001349348.2:c.-57-81A= NP_001336277.1:n.-57-81A=