Canonical Allele Identifier: CA1777236857

Gene: PLPBP

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765522G= , CM000670.2:g.37765522G=	GRCh38
NC_000008.10:g.37623040G= , CM000670.1:g.37623040G=	GRCh37
NC_000008.9:g.37742198G=	NCBI36
NG_053030.1:g.8770G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.100-4G= MANE Select	ENSP00000333551.3:n.100-4G=
ENST00000328195.7:c.100-4G=	ENSP00000333551.3:n.100-4G=
ENST00000518036.5:c.100-4G=	ENSP00000428005.1:n.100-4G=
ENST00000520073.5:n.165-4G=
ENST00000523187.5:c.-57-4G=	ENSP00000427886.1:n.-57-4G=
ENST00000523358.5:c.100-4G=	ENSP00000427778.1:n.100-4G=
ENST00000523994.1:n.105-4G=
NM_007198.3:c.100-4G=	NP_009129.1:n.100-4G=
NM_001349346.1:c.100-4G=	NP_001336275.1:n.100-4G=
NM_001349347.1:c.100-4G=	NP_001336276.1:n.100-4G=
NM_001349348.1:c.-57-4G=	NP_001336277.1:n.-57-4G=
NM_001349349.1:c.205-4G=	NP_001336278.1:n.205-4G=
NM_007198.4:c.100-4G= MANE Select	NP_009129.1:n.100-4G=
NM_001349346.2:c.100-4G=	NP_001336275.1:n.100-4G=
NM_001349347.2:c.100-4G=	NP_001336276.1:n.100-4G=
NM_001349348.2:c.-57-4G=	NP_001336277.1:n.-57-4G=