Canonical Allele Identifier: CA581101113

Gene: PLPBP

Linked Data

• dbSNP Id: rs1244950402
• gnomAD v2: 8-37623207-T-G
• gnomAD v4: 8-37765689-T-G
• MyVariant Identifiers: chr8:g.37623207T>G (hg19) ; chr8:g.37765689T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765689T>G , CM000670.2:g.37765689T>G	GRCh38
NC_000008.10:g.37623207T>G , CM000670.1:g.37623207T>G	GRCh37
NC_000008.9:g.37742365T>G	NCBI36
NG_053030.1:g.8937T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.208-22T>G MANE Select	ENSP00000333551.3:n.208-22T>G
ENST00000328195.7:c.208-22T>G	ENSP00000333551.3:n.208-22T>G
ENST00000518036.5:c.*38T>G	ENSP00000428005.1:n.*38T>G
ENST00000520073.5:n.273-22T>G
ENST00000523187.5:c.52-22T>G	ENSP00000427886.1:n.52-22T>G
ENST00000523358.5:c.208-22T>G	ENSP00000427778.1:n.208-22T>G
ENST00000523994.1:n.213-22T>G
NM_007198.3:c.208-22T>G	NP_009129.1:n.208-22T>G
NM_001349346.1:c.208-22T>G	NP_001336275.1:n.208-22T>G
NM_001349347.1:c.208-28T>G	NP_001336276.1:n.208-28T>G
NM_001349348.1:c.52-22T>G	NP_001336277.1:n.52-22T>G
NM_001349349.1:c.313-22T>G	NP_001336278.1:n.313-22T>G
NM_007198.4:c.208-22T>G MANE Select	NP_009129.1:n.208-22T>G
NM_001349346.2:c.208-22T>G	NP_001336275.1:n.208-22T>G
NM_001349347.2:c.208-28T>G	NP_001336276.1:n.208-28T>G
NM_001349348.2:c.52-22T>G	NP_001336277.1:n.52-22T>G