Canonical Allele Identifier: CA370666827

Gene: PLPBP

Linked Data

• MyVariant Identifiers: chr8:g.37623239T>A (hg19) ; chr8:g.37765721T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765721T>A , CM000670.2:g.37765721T>A	GRCh38
NC_000008.10:g.37623239T>A , CM000670.1:g.37623239T>A	GRCh37
NC_000008.9:g.37742397T>A	NCBI36
NG_053030.1:g.8969T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.218T>A MANE Select	ENSP00000333551.3:p.Leu73Gln
ENST00000328195.7:c.218T>A	ENSP00000333551.3:p.Leu73Gln
ENST00000518036.5:c.*70T>A	ENSP00000428005.1:n.*70T>A
ENST00000520073.5:n.283T>A
ENST00000523187.5:c.62T>A	ENSP00000427886.1:p.Leu21Gln
ENST00000523358.5:c.218T>A	ENSP00000427778.1:p.Leu73Gln
ENST00000523994.1:n.223T>A
NM_007198.3:c.218T>A	NP_009129.1:p.Leu73Gln
NM_001349346.1:c.218T>A	NP_001336275.1:p.Leu73Gln
NM_001349347.1:c.212T>A	NP_001336276.1:p.Leu71Gln
NM_001349348.1:c.62T>A	NP_001336277.1:p.Leu21Gln
NM_001349349.1:c.323T>A	NP_001336278.1:p.Leu108Gln
NM_007198.4:c.218T>A MANE Select	NP_009129.1:p.Leu73Gln
NM_001349346.2:c.218T>A	NP_001336275.1:p.Leu73Gln
NM_001349347.2:c.212T>A	NP_001336276.1:p.Leu71Gln
NM_001349348.2:c.62T>A	NP_001336277.1:p.Leu21Gln