Canonical Allele Identifier: CA370666738

Gene: PLPBP

Linked Data

• MyVariant Identifiers: chr8:g.37623128C>G (hg19) ; chr8:g.37765610C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765610C>G , CM000670.2:g.37765610C>G	GRCh38
NC_000008.10:g.37623128C>G , CM000670.1:g.37623128C>G	GRCh37
NC_000008.9:g.37742286C>G	NCBI36
NG_053030.1:g.8858C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.184C>G MANE Select	ENSP00000333551.3:p.Gln62Glu
ENST00000328195.7:c.184C>G	ENSP00000333551.3:p.Gln62Glu
ENST00000518036.5:c.184C>G	ENSP00000428005.1:p.Gln62Glu
ENST00000520073.5:n.249C>G
ENST00000523187.5:c.28C>G	ENSP00000427886.1:p.Gln10Glu
ENST00000523358.5:c.184C>G	ENSP00000427778.1:p.Gln62Glu
ENST00000523994.1:n.189C>G
NM_007198.3:c.184C>G	NP_009129.1:p.Gln62Glu
NM_001349346.1:c.184C>G	NP_001336275.1:p.Gln62Glu
NM_001349347.1:c.184C>G	NP_001336276.1:p.Gln62Glu
NM_001349348.1:c.28C>G	NP_001336277.1:p.Gln10Glu
NM_001349349.1:c.289C>G	NP_001336278.1:p.Gln97Glu
NM_007198.4:c.184C>G MANE Select	NP_009129.1:p.Gln62Glu
NM_001349346.2:c.184C>G	NP_001336275.1:p.Gln62Glu
NM_001349347.2:c.184C>G	NP_001336276.1:p.Gln62Glu
NM_001349348.2:c.28C>G	NP_001336277.1:p.Gln10Glu