Canonical Allele Identifier: CA1777236937
Gene: PLPBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37765738A= , CM000670.2:g.37765738A= GRCh38
NC_000008.10:g.37623256A= , CM000670.1:g.37623256A= GRCh37
NC_000008.9:g.37742414A= NCBI36
NG_053030.1:g.8986A=

Transcript Alleles

HGVS Amino-acid change
ENST00000328195.8:c.235A= MANE Select ENSP00000333551.3:p.Asn79=
ENST00000328195.7:c.235A= ENSP00000333551.3:p.Asn79=
ENST00000518036.5:c.*87A= ENSP00000428005.1:n.*87A=
ENST00000520073.5:n.300A=
ENST00000523187.5:c.79A= ENSP00000427886.1:p.Asn27=
ENST00000523358.5:c.235A= ENSP00000427778.1:p.Asn79=
ENST00000523994.1:n.240A=
NM_007198.3:c.235A= NP_009129.1:p.Asn79=
NM_001349346.1:c.235A= NP_001336275.1:p.Asn79=
NM_001349347.1:c.229A= NP_001336276.1:p.Asn77=
NM_001349348.1:c.79A= NP_001336277.1:p.Asn27=
NM_001349349.1:c.340A= NP_001336278.1:p.Asn114=
NM_007198.4:c.235A= MANE Select NP_009129.1:p.Asn79=
NM_001349346.2:c.235A= NP_001336275.1:p.Asn79=
NM_001349347.2:c.229A= NP_001336276.1:p.Asn77=
NM_001349348.2:c.79A= NP_001336277.1:p.Asn27=