Canonical Allele Identifier: CA2686899557
Gene: PLPBP HGNC NCBI

Linked Data

gnomAD v4: 8-37765749-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37765749A>G , CM000670.2:g.37765749A>G GRCh38
NC_000008.10:g.37623267A>G , CM000670.1:g.37623267A>G GRCh37
NC_000008.9:g.37742425A>G NCBI36
NG_053030.1:g.8997A>G

Transcript Alleles

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