Canonical Allele Identifier: CA2716949616
Gene: PLPBP HGNC NCBI

Linked Data

dbSNP Id: rs2129775646

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37765816C>T , CM000670.2:g.37765816C>T GRCh38
NC_000008.10:g.37623334C>T , CM000670.1:g.37623334C>T GRCh37
NC_000008.9:g.37742492C>T NCBI36
NG_053030.1:g.9064C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000328195.8:c.243+70C>T MANE Select ENSP00000333551.3:n.243+70C>T
ENST00000328195.7:c.243+70C>T ENSP00000333551.3:n.243+70C>T
ENST00000518036.5:c.*95+70C>T ENSP00000428005.1:n.*95+70C>T
ENST00000520073.5:n.308+70C>T
ENST00000523187.5:c.87+70C>T ENSP00000427886.1:n.87+70C>T
ENST00000523358.5:c.243+70C>T ENSP00000427778.1:n.243+70C>T
ENST00000523994.1:n.248+70C>T
NM_007198.3:c.243+70C>T NP_009129.1:n.243+70C>T
NM_001349346.1:c.243+70C>T NP_001336275.1:n.243+70C>T
NM_001349347.1:c.237+70C>T NP_001336276.1:n.237+70C>T
NM_001349348.1:c.87+70C>T NP_001336277.1:n.87+70C>T
NM_001349349.1:c.348+70C>T NP_001336278.1:n.348+70C>T
NM_007198.4:c.243+70C>T MANE Select NP_009129.1:n.243+70C>T
NM_001349346.2:c.243+70C>T NP_001336275.1:n.243+70C>T
NM_001349347.2:c.237+70C>T NP_001336276.1:n.237+70C>T
NM_001349348.2:c.87+70C>T NP_001336277.1:n.87+70C>T