Canonical Allele Identifier: CA2686899438

Gene: PLPBP

Linked Data

• gnomAD v4: 8-37765648-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37765648C>G , CM000670.2:g.37765648C>G	GRCh38
NC_000008.10:g.37623166C>G , CM000670.1:g.37623166C>G	GRCh37
NC_000008.9:g.37742324C>G	NCBI36
NG_053030.1:g.8896C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000328195.8:c.207+15C>G MANE Select	ENSP00000333551.3:n.207+15C>G
ENST00000328195.7:c.207+15C>G	ENSP00000333551.3:n.207+15C>G
ENST00000518036.5:c.222C>G	ENSP00000428005.1:p.Ser74=
ENST00000520073.5:n.272+15C>G
ENST00000523187.5:c.51+15C>G	ENSP00000427886.1:n.51+15C>G
ENST00000523358.5:c.207+15C>G	ENSP00000427778.1:n.207+15C>G
ENST00000523994.1:n.212+15C>G
NM_007198.3:c.207+15C>G	NP_009129.1:n.207+15C>G
NM_001349346.1:c.207+15C>G	NP_001336275.1:n.207+15C>G
NM_001349347.1:c.207+15C>G	NP_001336276.1:n.207+15C>G
NM_001349348.1:c.51+15C>G	NP_001336277.1:n.51+15C>G
NM_001349349.1:c.312+15C>G	NP_001336278.1:n.312+15C>G
NM_007198.4:c.207+15C>G MANE Select	NP_009129.1:n.207+15C>G
NM_001349346.2:c.207+15C>G	NP_001336275.1:n.207+15C>G
NM_001349347.2:c.207+15C>G	NP_001336276.1:n.207+15C>G
NM_001349348.2:c.51+15C>G	NP_001336277.1:n.51+15C>G