Canonical Allele Identifier: CA2779755741
Gene: PLPBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37765696G>C , CM000670.2:g.37765696G>C GRCh38
NC_000008.10:g.37623214G>C , CM000670.1:g.37623214G>C GRCh37
NC_000008.9:g.37742372G>C NCBI36
NG_053030.1:g.8944G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000328195.8:c.208-15G>C MANE Select ENSP00000333551.3:n.208-15G>C
ENST00000328195.7:c.208-15G>C ENSP00000333551.3:n.208-15G>C
ENST00000518036.5:c.*45G>C ENSP00000428005.1:n.*45G>C
ENST00000520073.5:n.273-15G>C
ENST00000523187.5:c.52-15G>C ENSP00000427886.1:n.52-15G>C
ENST00000523358.5:c.208-15G>C ENSP00000427778.1:n.208-15G>C
ENST00000523994.1:n.213-15G>C
NM_007198.3:c.208-15G>C NP_009129.1:n.208-15G>C
NM_001349346.1:c.208-15G>C NP_001336275.1:n.208-15G>C
NM_001349347.1:c.208-21G>C NP_001336276.1:n.208-21G>C
NM_001349348.1:c.52-15G>C NP_001336277.1:n.52-15G>C
NM_001349349.1:c.313-15G>C NP_001336278.1:n.313-15G>C
NM_007198.4:c.208-15G>C MANE Select NP_009129.1:n.208-15G>C
NM_001349346.2:c.208-15G>C NP_001336275.1:n.208-15G>C
NM_001349347.2:c.208-21G>C NP_001336276.1:n.208-21G>C
NM_001349348.2:c.52-15G>C NP_001336277.1:n.52-15G>C