Canonical Allele Identifier: CA370666620
Gene: PLPBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37765568A>G , CM000670.2:g.37765568A>G GRCh38
NC_000008.10:g.37623086A>G , CM000670.1:g.37623086A>G GRCh37
NC_000008.9:g.37742244A>G NCBI36
NG_053030.1:g.8816A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000328195.8:c.142A>G MANE Select ENSP00000333551.3:p.Thr48Ala
ENST00000328195.7:c.142A>G ENSP00000333551.3:p.Thr48Ala
ENST00000518036.5:c.142A>G ENSP00000428005.1:p.Thr48Ala
ENST00000520073.5:n.207A>G
ENST00000523187.5:c.-15A>G ENSP00000427886.1:n.-15A>G
ENST00000523358.5:c.142A>G ENSP00000427778.1:p.Thr48Ala
ENST00000523994.1:n.147A>G
NM_007198.3:c.142A>G NP_009129.1:p.Thr48Ala
NM_001349346.1:c.142A>G NP_001336275.1:p.Thr48Ala
NM_001349347.1:c.142A>G NP_001336276.1:p.Thr48Ala
NM_001349348.1:c.-15A>G NP_001336277.1:n.-15A>G
NM_001349349.1:c.247A>G NP_001336278.1:p.Thr83Ala
NM_007198.4:c.142A>G MANE Select NP_009129.1:p.Thr48Ala
NM_001349346.2:c.142A>G NP_001336275.1:p.Thr48Ala
NM_001349347.2:c.142A>G NP_001336276.1:p.Thr48Ala
NM_001349348.2:c.-15A>G NP_001336277.1:n.-15A>G