Canonical Allele Identifier: CA1777236864

Gene: PLPBP

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765543G= , CM000670.2:g.37765543G=	GRCh38
NC_000008.10:g.37623061G= , CM000670.1:g.37623061G=	GRCh37
NC_000008.9:g.37742219G=	NCBI36
NG_053030.1:g.8791G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.117G= MANE Select	ENSP00000333551.3:p.Gln39=
ENST00000328195.7:c.117G=	ENSP00000333551.3:p.Gln39=
ENST00000518036.5:c.117G=	ENSP00000428005.1:p.Gln39=
ENST00000520073.5:n.182G=
ENST00000523187.5:c.-40G=	ENSP00000427886.1:n.-40G=
ENST00000523358.5:c.117G=	ENSP00000427778.1:p.Gln39=
ENST00000523994.1:n.122G=
NM_007198.3:c.117G=	NP_009129.1:p.Gln39=
NM_001349346.1:c.117G=	NP_001336275.1:p.Gln39=
NM_001349347.1:c.117G=	NP_001336276.1:p.Gln39=
NM_001349348.1:c.-40G=	NP_001336277.1:n.-40G=
NM_001349349.1:c.222G=	NP_001336278.1:p.Gln74=
NM_007198.4:c.117G= MANE Select	NP_009129.1:p.Gln39=
NM_001349346.2:c.117G=	NP_001336275.1:p.Gln39=
NM_001349347.2:c.117G=	NP_001336276.1:p.Gln39=
NM_001349348.2:c.-40G=	NP_001336277.1:n.-40G=