Canonical Allele Identifier: CA370666565
Gene: PLPBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37765556G>T , CM000670.2:g.37765556G>T GRCh38
NC_000008.10:g.37623074G>T , CM000670.1:g.37623074G>T GRCh37
NC_000008.9:g.37742232G>T NCBI36
NG_053030.1:g.8804G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000328195.8:c.130G>T MANE Select ENSP00000333551.3:p.Ala44Ser
ENST00000328195.7:c.130G>T ENSP00000333551.3:p.Ala44Ser
ENST00000518036.5:c.130G>T ENSP00000428005.1:p.Ala44Ser
ENST00000520073.5:n.195G>T
ENST00000523187.5:c.-27G>T ENSP00000427886.1:n.-27G>T
ENST00000523358.5:c.130G>T ENSP00000427778.1:p.Ala44Ser
ENST00000523994.1:n.135G>T
NM_007198.3:c.130G>T NP_009129.1:p.Ala44Ser
NM_001349346.1:c.130G>T NP_001336275.1:p.Ala44Ser
NM_001349347.1:c.130G>T NP_001336276.1:p.Ala44Ser
NM_001349348.1:c.-27G>T NP_001336277.1:n.-27G>T
NM_001349349.1:c.235G>T NP_001336278.1:p.Ala79Ser
NM_007198.4:c.130G>T MANE Select NP_009129.1:p.Ala44Ser
NM_001349346.2:c.130G>T NP_001336275.1:p.Ala44Ser
NM_001349347.2:c.130G>T NP_001336276.1:p.Ala44Ser
NM_001349348.2:c.-27G>T NP_001336277.1:n.-27G>T