Canonical Allele Identifier: CA370667914

Gene: PLPBP

Linked Data

• MyVariant Identifiers: chr8:g.37630384A>G (hg19) ; chr8:g.37772866A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37772866A>G , CM000670.2:g.37772866A>G	GRCh38
NC_000008.10:g.37630384A>G , CM000670.1:g.37630384A>G	GRCh37
NC_000008.9:g.37749542A>G	NCBI36
NG_053030.1:g.16114A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.431A>G MANE Select	ENSP00000333551.3:p.Gln144Arg
ENST00000328195.7:c.431A>G	ENSP00000333551.3:p.Gln144Arg
ENST00000518036.5:c.*283A>G	ENSP00000428005.1:n.*283A>G
ENST00000521631.1:n.114A>G
ENST00000523187.5:c.275A>G	ENSP00000427886.1:p.Gln92Arg
ENST00000523358.5:c.431A>G	ENSP00000427778.1:p.Gln144Arg
ENST00000523521.1:c.188A>G	ENSP00000429425.1:p.Gln63Arg
NM_007198.3:c.431A>G	NP_009129.1:p.Gln144Arg
NM_001349346.1:c.431A>G	NP_001336275.1:p.Gln144Arg
NM_001349347.1:c.425A>G	NP_001336276.1:p.Gln142Arg
NM_001349348.1:c.275A>G	NP_001336277.1:p.Gln92Arg
NM_007198.4:c.431A>G MANE Select	NP_009129.1:p.Gln144Arg
NM_001349346.2:c.431A>G	NP_001336275.1:p.Gln144Arg
NM_001349347.2:c.425A>G	NP_001336276.1:p.Gln142Arg
NM_001349348.2:c.275A>G	NP_001336277.1:p.Gln92Arg