Canonical Allele Identifier: CA1777236889

Gene: PLPBP

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765600T= , CM000670.2:g.37765600T=	GRCh38
NC_000008.10:g.37623118T= , CM000670.1:g.37623118T=	GRCh37
NC_000008.9:g.37742276T=	NCBI36
NG_053030.1:g.8848T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.174T= MANE Select	ENSP00000333551.3:p.Tyr58=
ENST00000328195.7:c.174T=	ENSP00000333551.3:p.Tyr58=
ENST00000518036.5:c.174T=	ENSP00000428005.1:p.Tyr58=
ENST00000520073.5:n.239T=
ENST00000523187.5:c.18T=	ENSP00000427886.1:p.Tyr6=
ENST00000523358.5:c.174T=	ENSP00000427778.1:p.Tyr58=
ENST00000523994.1:n.179T=
NM_007198.3:c.174T=	NP_009129.1:p.Tyr58=
NM_001349346.1:c.174T=	NP_001336275.1:p.Tyr58=
NM_001349347.1:c.174T=	NP_001336276.1:p.Tyr58=
NM_001349348.1:c.18T=	NP_001336277.1:p.Tyr6=
NM_001349349.1:c.279T=	NP_001336278.1:p.Tyr93=
NM_007198.4:c.174T= MANE Select	NP_009129.1:p.Tyr58=
NM_001349346.2:c.174T=	NP_001336275.1:p.Tyr58=
NM_001349347.2:c.174T=	NP_001336276.1:p.Tyr58=
NM_001349348.2:c.18T=	NP_001336277.1:p.Tyr6=