Canonical Allele Identifier: CA1777240082

Gene: PLPBP

Linked Data

• dbSNP Id: rs1803812572
• gnomAD v4: 8-37772894-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.37772894G>C , CM000670.2:g.37772894G>C	GRCh38
NC_000008.10:g.37630412G>C , CM000670.1:g.37630412G>C	GRCh37
NC_000008.9:g.37749570G>C	NCBI36
NG_053030.1:g.16142G>C

Transcript Alleles

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