Canonical Allele Identifier: CA370666730

Gene: PLPBP

Linked Data

• MyVariant Identifiers: chr8:g.37623124T>A (hg19) ; chr8:g.37765606T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765606T>A , CM000670.2:g.37765606T>A	GRCh38
NC_000008.10:g.37623124T>A , CM000670.1:g.37623124T>A	GRCh37
NC_000008.9:g.37742282T>A	NCBI36
NG_053030.1:g.8854T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.180T>A MANE Select	ENSP00000333551.3:p.His60Gln
ENST00000328195.7:c.180T>A	ENSP00000333551.3:p.His60Gln
ENST00000518036.5:c.180T>A	ENSP00000428005.1:p.His60Gln
ENST00000520073.5:n.245T>A
ENST00000523187.5:c.24T>A	ENSP00000427886.1:p.His8Gln
ENST00000523358.5:c.180T>A	ENSP00000427778.1:p.His60Gln
ENST00000523994.1:n.185T>A
NM_007198.3:c.180T>A	NP_009129.1:p.His60Gln
NM_001349346.1:c.180T>A	NP_001336275.1:p.His60Gln
NM_001349347.1:c.180T>A	NP_001336276.1:p.His60Gln
NM_001349348.1:c.24T>A	NP_001336277.1:p.His8Gln
NM_001349349.1:c.285T>A	NP_001336278.1:p.His95Gln
NM_007198.4:c.180T>A MANE Select	NP_009129.1:p.His60Gln
NM_001349346.2:c.180T>A	NP_001336275.1:p.His60Gln
NM_001349347.2:c.180T>A	NP_001336276.1:p.His60Gln
NM_001349348.2:c.24T>A	NP_001336277.1:p.His8Gln