Canonical Allele Identifier: CA370667918

Gene: PLPBP

Linked Data

• MyVariant Identifiers: chr8:g.37630386A>G (hg19) ; chr8:g.37772868A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37772868A>G , CM000670.2:g.37772868A>G	GRCh38
NC_000008.10:g.37630386A>G , CM000670.1:g.37630386A>G	GRCh37
NC_000008.9:g.37749544A>G	NCBI36
NG_053030.1:g.16116A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.433A>G MANE Select	ENSP00000333551.3:p.Ile145Val
ENST00000328195.7:c.433A>G	ENSP00000333551.3:p.Ile145Val
ENST00000521631.1:n.116A>G
ENST00000523187.5:c.277A>G	ENSP00000427886.1:p.Ile93Val
ENST00000523358.5:c.433A>G	ENSP00000427778.1:p.Ile145Val
ENST00000523521.1:c.190A>G	ENSP00000429425.1:p.Ile64Val
NM_007198.3:c.433A>G	NP_009129.1:p.Ile145Val
NM_001349346.1:c.433A>G	NP_001336275.1:p.Ile145Val
NM_001349347.1:c.427A>G	NP_001336276.1:p.Ile143Val
NM_001349348.1:c.277A>G	NP_001336277.1:p.Ile93Val
NM_007198.4:c.433A>G MANE Select	NP_009129.1:p.Ile145Val
NM_001349346.2:c.433A>G	NP_001336275.1:p.Ile145Val
NM_001349347.2:c.427A>G	NP_001336276.1:p.Ile143Val
NM_001349348.2:c.277A>G	NP_001336277.1:p.Ile93Val