Canonical Allele Identifier: CA1777236910
Gene: PLPBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37765648C= , CM000670.2:g.37765648C= GRCh38
NC_000008.10:g.37623166C= , CM000670.1:g.37623166C= GRCh37
NC_000008.9:g.37742324C= NCBI36
NG_053030.1:g.8896C=

Transcript Alleles

HGVS Amino-acid change
ENST00000328195.8:c.207+15C= MANE Select ENSP00000333551.3:n.207+15C=
ENST00000328195.7:c.207+15C= ENSP00000333551.3:n.207+15C=
ENST00000518036.5:c.222C= ENSP00000428005.1:p.Ser74=
ENST00000520073.5:n.272+15C=
ENST00000523187.5:c.51+15C= ENSP00000427886.1:n.51+15C=
ENST00000523358.5:c.207+15C= ENSP00000427778.1:n.207+15C=
ENST00000523994.1:n.212+15C=
NM_007198.3:c.207+15C= NP_009129.1:n.207+15C=
NM_001349346.1:c.207+15C= NP_001336275.1:n.207+15C=
NM_001349347.1:c.207+15C= NP_001336276.1:n.207+15C=
NM_001349348.1:c.51+15C= NP_001336277.1:n.51+15C=
NM_001349349.1:c.312+15C= NP_001336278.1:n.312+15C=
NM_007198.4:c.207+15C= MANE Select NP_009129.1:n.207+15C=
NM_001349346.2:c.207+15C= NP_001336275.1:n.207+15C=
NM_001349347.2:c.207+15C= NP_001336276.1:n.207+15C=
NM_001349348.2:c.51+15C= NP_001336277.1:n.51+15C=