Canonical Allele Identifier: CA2686899656
Gene: PLPBP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37765801_37765802insCCACCG , CM000670.2:g.37765801_37765802insCCACCG GRCh38
NC_000008.10:g.37623319_37623320insCCACCG , CM000670.1:g.37623319_37623320insCCACCG GRCh37
NC_000008.9:g.37742477_37742478insCCACCG NCBI36
NG_053030.1:g.9049_9050insCCACCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000328195.8:c.243+55_243+56insCCACCG MANE Select ENSP00000333551.3:n.243+55_243+56insCCACCG
ENST00000328195.7:c.243+55_243+56insCCACCG ENSP00000333551.3:n.243+55_243+56insCCACCG
ENST00000518036.5:c.*95+55_*95+56insCCACCG ENSP00000428005.1:n.*95+55_*95+56insCCACCG
ENST00000520073.5:n.308+55_308+56insCCACCG
ENST00000523187.5:c.87+55_87+56insCCACCG ENSP00000427886.1:n.87+55_87+56insCCACCG
ENST00000523358.5:c.243+55_243+56insCCACCG ENSP00000427778.1:n.243+55_243+56insCCACCG
ENST00000523994.1:n.248+55_248+56insCCACCG
NM_007198.3:c.243+55_243+56insCCACCG NP_009129.1:n.243+55_243+56insCCACCG
NM_001349346.1:c.243+55_243+56insCCACCG NP_001336275.1:n.243+55_243+56insCCACCG
NM_001349347.1:c.237+55_237+56insCCACCG NP_001336276.1:n.237+55_237+56insCCACCG
NM_001349348.1:c.87+55_87+56insCCACCG NP_001336277.1:n.87+55_87+56insCCACCG
NM_001349349.1:c.348+55_348+56insCCACCG NP_001336278.1:n.348+55_348+56insCCACCG
NM_007198.4:c.243+55_243+56insCCACCG MANE Select NP_009129.1:n.243+55_243+56insCCACCG
NM_001349346.2:c.243+55_243+56insCCACCG NP_001336275.1:n.243+55_243+56insCCACCG
NM_001349347.2:c.237+55_237+56insCCACCG NP_001336276.1:n.237+55_237+56insCCACCG
NM_001349348.2:c.87+55_87+56insCCACCG NP_001336277.1:n.87+55_87+56insCCACCG