Canonical Allele Identifier: CA370666858

Gene: PLPBP

Linked Data

• MyVariant Identifiers: chr8:g.37623253T>C (hg19) ; chr8:g.37765735T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765735T>C , CM000670.2:g.37765735T>C	GRCh38
NC_000008.10:g.37623253T>C , CM000670.1:g.37623253T>C	GRCh37
NC_000008.9:g.37742411T>C	NCBI36
NG_053030.1:g.8983T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.232T>C MANE Select	ENSP00000333551.3:p.Ser78Pro
ENST00000328195.7:c.232T>C	ENSP00000333551.3:p.Ser78Pro
ENST00000518036.5:c.*84T>C	ENSP00000428005.1:n.*84T>C
ENST00000520073.5:n.297T>C
ENST00000523187.5:c.76T>C	ENSP00000427886.1:p.Ser26Pro
ENST00000523358.5:c.232T>C	ENSP00000427778.1:p.Ser78Pro
ENST00000523994.1:n.237T>C
NM_007198.3:c.232T>C	NP_009129.1:p.Ser78Pro
NM_001349346.1:c.232T>C	NP_001336275.1:p.Ser78Pro
NM_001349347.1:c.226T>C	NP_001336276.1:p.Ser76Pro
NM_001349348.1:c.76T>C	NP_001336277.1:p.Ser26Pro
NM_001349349.1:c.337T>C	NP_001336278.1:p.Ser113Pro
NM_007198.4:c.232T>C MANE Select	NP_009129.1:p.Ser78Pro
NM_001349346.2:c.232T>C	NP_001336275.1:p.Ser78Pro
NM_001349347.2:c.226T>C	NP_001336276.1:p.Ser76Pro
NM_001349348.2:c.76T>C	NP_001336277.1:p.Ser26Pro