Canonical Allele Identifier: CA370666552

Gene: PLPBP

Linked Data

• MyVariant Identifiers: chr8:g.37623071G>A (hg19) ; chr8:g.37765553G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765553G>A , CM000670.2:g.37765553G>A	GRCh38
NC_000008.10:g.37623071G>A , CM000670.1:g.37623071G>A	GRCh37
NC_000008.9:g.37742229G>A	NCBI36
NG_053030.1:g.8801G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.127G>A MANE Select	ENSP00000333551.3:p.Val43Met
ENST00000328195.7:c.127G>A	ENSP00000333551.3:p.Val43Met
ENST00000518036.5:c.127G>A	ENSP00000428005.1:p.Val43Met
ENST00000520073.5:n.192G>A
ENST00000523187.5:c.-30G>A	ENSP00000427886.1:n.-30G>A
ENST00000523358.5:c.127G>A	ENSP00000427778.1:p.Val43Met
ENST00000523994.1:n.132G>A
NM_007198.3:c.127G>A	NP_009129.1:p.Val43Met
NM_001349346.1:c.127G>A	NP_001336275.1:p.Val43Met
NM_001349347.1:c.127G>A	NP_001336276.1:p.Val43Met
NM_001349348.1:c.-30G>A	NP_001336277.1:n.-30G>A
NM_001349349.1:c.232G>A	NP_001336278.1:p.Val78Met
NM_007198.4:c.127G>A MANE Select	NP_009129.1:p.Val43Met
NM_001349346.2:c.127G>A	NP_001336275.1:p.Val43Met
NM_001349347.2:c.127G>A	NP_001336276.1:p.Val43Met
NM_001349348.2:c.-30G>A	NP_001336277.1:n.-30G>A