Canonical Allele Identifier: CA370666628

Gene: PLPBP

Linked Data

• MyVariant Identifiers: chr8:g.37623087C>T (hg19) ; chr8:g.37765569C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765569C>T , CM000670.2:g.37765569C>T	GRCh38
NC_000008.10:g.37623087C>T , CM000670.1:g.37623087C>T	GRCh37
NC_000008.9:g.37742245C>T	NCBI36
NG_053030.1:g.8817C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.143C>T MANE Select	ENSP00000333551.3:p.Thr48Ile
ENST00000328195.7:c.143C>T	ENSP00000333551.3:p.Thr48Ile
ENST00000518036.5:c.143C>T	ENSP00000428005.1:p.Thr48Ile
ENST00000520073.5:n.208C>T
ENST00000523187.5:c.-14C>T	ENSP00000427886.1:n.-14C>T
ENST00000523358.5:c.143C>T	ENSP00000427778.1:p.Thr48Ile
ENST00000523994.1:n.148C>T
NM_007198.3:c.143C>T	NP_009129.1:p.Thr48Ile
NM_001349346.1:c.143C>T	NP_001336275.1:p.Thr48Ile
NM_001349347.1:c.143C>T	NP_001336276.1:p.Thr48Ile
NM_001349348.1:c.-14C>T	NP_001336277.1:n.-14C>T
NM_001349349.1:c.248C>T	NP_001336278.1:p.Thr83Ile
NM_007198.4:c.143C>T MANE Select	NP_009129.1:p.Thr48Ile
NM_001349346.2:c.143C>T	NP_001336275.1:p.Thr48Ile
NM_001349347.2:c.143C>T	NP_001336276.1:p.Thr48Ile
NM_001349348.2:c.-14C>T	NP_001336277.1:n.-14C>T