Canonical Allele Identifier: CA460358951

Gene: PLPBP

Linked Data

• MyVariant Identifiers: chr8:g.37623067G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765549G>C , CM000670.2:g.37765549G>C	GRCh38
NC_000008.10:g.37623067G>C , CM000670.1:g.37623067G>C	GRCh37
NC_000008.9:g.37742225G>C	NCBI36
NG_053030.1:g.8797G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.123G>C MANE Select	ENSP00000333551.3:p.Arg41=
ENST00000328195.7:c.123G>C	ENSP00000333551.3:p.Arg41=
ENST00000518036.5:c.123G>C	ENSP00000428005.1:p.Arg41=
ENST00000520073.5:n.188G>C
ENST00000523187.5:c.-34G>C	ENSP00000427886.1:n.-34G>C
ENST00000523358.5:c.123G>C	ENSP00000427778.1:p.Arg41=
ENST00000523994.1:n.128G>C
NM_007198.3:c.123G>C	NP_009129.1:p.Arg41=
NM_001349346.1:c.123G>C	NP_001336275.1:p.Arg41=
NM_001349347.1:c.123G>C	NP_001336276.1:p.Arg41=
NM_001349348.1:c.-34G>C	NP_001336277.1:n.-34G>C
NM_001349349.1:c.228G>C	NP_001336278.1:p.Arg76=
NM_007198.4:c.123G>C MANE Select	NP_009129.1:p.Arg41=
NM_001349346.2:c.123G>C	NP_001336275.1:p.Arg41=
NM_001349347.2:c.123G>C	NP_001336276.1:p.Arg41=
NM_001349348.2:c.-34G>C	NP_001336277.1:n.-34G>C