Canonical Allele Identifier: CA2686899800

Gene: PLPBP

Linked Data

• gnomAD v4: 8-37765898-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765898C>A , CM000670.2:g.37765898C>A	GRCh38
NC_000008.10:g.37623416C>A , CM000670.1:g.37623416C>A	GRCh37
NC_000008.9:g.37742574C>A	NCBI36
NG_053030.1:g.9146C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.243+152C>A MANE Select	ENSP00000333551.3:n.243+152C>A
ENST00000328195.7:c.243+152C>A	ENSP00000333551.3:n.243+152C>A
ENST00000518036.5:c.*95+152C>A	ENSP00000428005.1:n.*95+152C>A
ENST00000520073.5:n.308+152C>A
ENST00000523187.5:c.87+152C>A	ENSP00000427886.1:n.87+152C>A
ENST00000523358.5:c.243+152C>A	ENSP00000427778.1:n.243+152C>A
ENST00000523994.1:n.248+152C>A
NM_007198.3:c.243+152C>A	NP_009129.1:n.243+152C>A
NM_001349346.1:c.243+152C>A	NP_001336275.1:n.243+152C>A
NM_001349347.1:c.237+152C>A	NP_001336276.1:n.237+152C>A
NM_001349348.1:c.87+152C>A	NP_001336277.1:n.87+152C>A
NM_001349349.1:c.348+152C>A	NP_001336278.1:n.348+152C>A
NM_007198.4:c.243+152C>A MANE Select	NP_009129.1:n.243+152C>A
NM_001349346.2:c.243+152C>A	NP_001336275.1:n.243+152C>A
NM_001349347.2:c.237+152C>A	NP_001336276.1:n.237+152C>A
NM_001349348.2:c.87+152C>A	NP_001336277.1:n.87+152C>A