Canonical Allele Identifier: CA1777236938

Gene: PLPBP

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765740T= , CM000670.2:g.37765740T=	GRCh38
NC_000008.10:g.37623258T= , CM000670.1:g.37623258T=	GRCh37
NC_000008.9:g.37742416T=	NCBI36
NG_053030.1:g.8988T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.237T= MANE Select	ENSP00000333551.3:p.Asn79=
ENST00000328195.7:c.237T=	ENSP00000333551.3:p.Asn79=
ENST00000518036.5:c.*89T=	ENSP00000428005.1:n.*89T=
ENST00000520073.5:n.302T=
ENST00000523187.5:c.81T=	ENSP00000427886.1:p.Asn27=
ENST00000523358.5:c.237T=	ENSP00000427778.1:p.Asn79=
ENST00000523994.1:n.242T=
NM_007198.3:c.237T=	NP_009129.1:p.Asn79=
NM_001349346.1:c.237T=	NP_001336275.1:p.Asn79=
NM_001349347.1:c.231T=	NP_001336276.1:p.Asn77=
NM_001349348.1:c.81T=	NP_001336277.1:p.Asn27=
NM_001349349.1:c.342T=	NP_001336278.1:p.Asn114=
NM_007198.4:c.237T= MANE Select	NP_009129.1:p.Asn79=
NM_001349346.2:c.237T=	NP_001336275.1:p.Asn79=
NM_001349347.2:c.231T=	NP_001336276.1:p.Asn77=
NM_001349348.2:c.81T=	NP_001336277.1:p.Asn27=