Canonical Allele Identifier: CA460359167

Gene: PLPBP

Linked Data

• MyVariant Identifiers: chr8:g.37630400A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37772882A>T , CM000670.2:g.37772882A>T	GRCh38
NC_000008.10:g.37630400A>T , CM000670.1:g.37630400A>T	GRCh37
NC_000008.9:g.37749558A>T	NCBI36
NG_053030.1:g.16130A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.447A>T MANE Select	ENSP00000333551.3:p.Gly149=
ENST00000328195.7:c.447A>T	ENSP00000333551.3:p.Gly149=
ENST00000521631.1:n.130A>T
ENST00000523187.5:c.291A>T	ENSP00000427886.1:p.Gly97=
ENST00000523358.5:c.447A>T	ENSP00000427778.1:p.Gly149=
ENST00000523521.1:c.204A>T	ENSP00000429425.1:p.Gly68=
NM_007198.3:c.447A>T	NP_009129.1:p.Gly149=
NM_001349346.1:c.447A>T	NP_001336275.1:p.Gly149=
NM_001349347.1:c.441A>T	NP_001336276.1:p.Gly147=
NM_001349348.1:c.291A>T	NP_001336277.1:p.Gly97=
NM_007198.4:c.447A>T MANE Select	NP_009129.1:p.Gly149=
NM_001349346.2:c.447A>T	NP_001336275.1:p.Gly149=
NM_001349347.2:c.441A>T	NP_001336276.1:p.Gly147=
NM_001349348.2:c.291A>T	NP_001336277.1:p.Gly97=