Canonical Allele Identifier: CA1777236876

Gene: PLPBP

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765571A= , CM000670.2:g.37765571A=	GRCh38
NC_000008.10:g.37623089A= , CM000670.1:g.37623089A=	GRCh37
NC_000008.9:g.37742247A=	NCBI36
NG_053030.1:g.8819A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.145A= MANE Select	ENSP00000333551.3:p.Lys49=
ENST00000328195.7:c.145A=	ENSP00000333551.3:p.Lys49=
ENST00000518036.5:c.145A=	ENSP00000428005.1:p.Lys49=
ENST00000520073.5:n.210A=
ENST00000523187.5:c.-12A=	ENSP00000427886.1:n.-12A=
ENST00000523358.5:c.145A=	ENSP00000427778.1:p.Lys49=
ENST00000523994.1:n.150A=
NM_007198.3:c.145A=	NP_009129.1:p.Lys49=
NM_001349346.1:c.145A=	NP_001336275.1:p.Lys49=
NM_001349347.1:c.145A=	NP_001336276.1:p.Lys49=
NM_001349348.1:c.-12A=	NP_001336277.1:n.-12A=
NM_001349349.1:c.250A=	NP_001336278.1:p.Lys84=
NM_007198.4:c.145A= MANE Select	NP_009129.1:p.Lys49=
NM_001349346.2:c.145A=	NP_001336275.1:p.Lys49=
NM_001349347.2:c.145A=	NP_001336276.1:p.Lys49=
NM_001349348.2:c.-12A=	NP_001336277.1:n.-12A=