Canonical Allele Identifier: CA460358991

Gene: PLPBP

Linked Data

• MyVariant Identifiers: chr8:g.37623130G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765612G>A , CM000670.2:g.37765612G>A	GRCh38
NC_000008.10:g.37623130G>A , CM000670.1:g.37623130G>A	GRCh37
NC_000008.9:g.37742288G>A	NCBI36
NG_053030.1:g.8860G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.186G>A MANE Select	ENSP00000333551.3:p.Gln62=
ENST00000328195.7:c.186G>A	ENSP00000333551.3:p.Gln62=
ENST00000518036.5:c.186G>A	ENSP00000428005.1:p.Gln62=
ENST00000520073.5:n.251G>A
ENST00000523187.5:c.30G>A	ENSP00000427886.1:p.Gln10=
ENST00000523358.5:c.186G>A	ENSP00000427778.1:p.Gln62=
ENST00000523994.1:n.191G>A
NM_007198.3:c.186G>A	NP_009129.1:p.Gln62=
NM_001349346.1:c.186G>A	NP_001336275.1:p.Gln62=
NM_001349347.1:c.186G>A	NP_001336276.1:p.Gln62=
NM_001349348.1:c.30G>A	NP_001336277.1:p.Gln10=
NM_001349349.1:c.291G>A	NP_001336278.1:p.Gln97=
NM_007198.4:c.186G>A MANE Select	NP_009129.1:p.Gln62=
NM_001349346.2:c.186G>A	NP_001336275.1:p.Gln62=
NM_001349347.2:c.186G>A	NP_001336276.1:p.Gln62=
NM_001349348.2:c.30G>A	NP_001336277.1:p.Gln10=