Canonical Allele Identifier: CA581101734

Gene: PLPBP

Linked Data

• dbSNP Id: rs1262835314
• gnomAD v2: 8-37630426-A-T
• gnomAD v4: 8-37772908-A-T
• MyVariant Identifiers: chr8:g.37630426A>T (hg19) ; chr8:g.37772908A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37772908A>T , CM000670.2:g.37772908A>T	GRCh38
NC_000008.10:g.37630426A>T , CM000670.1:g.37630426A>T	GRCh37
NC_000008.9:g.37749584A>T	NCBI36
NG_053030.1:g.16156A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328195.8:c.454+19A>T MANE Select	ENSP00000333551.3:n.454+19A>T
ENST00000328195.7:c.454+19A>T	ENSP00000333551.3:n.454+19A>T
ENST00000521631.1:n.137+19A>T
ENST00000523187.5:c.298+19A>T	ENSP00000427886.1:n.298+19A>T
ENST00000523521.1:c.211+19A>T	ENSP00000429425.1:n.211+19A>T
NM_007198.3:c.454+19A>T	NP_009129.1:n.454+19A>T
NM_001349346.1:c.454+19A>T	NP_001336275.1:n.454+19A>T
NM_001349347.1:c.448+19A>T	NP_001336276.1:n.448+19A>T
NM_001349348.1:c.298+19A>T	NP_001336277.1:n.298+19A>T
NM_007198.4:c.454+19A>T MANE Select	NP_009129.1:n.454+19A>T
NM_001349346.2:c.454+19A>T	NP_001336275.1:n.454+19A>T
NM_001349347.2:c.448+19A>T	NP_001336276.1:n.448+19A>T
NM_001349348.2:c.298+19A>T	NP_001336277.1:n.298+19A>T