Canonical Allele Identifier: CA313304333
Gene: PXMP4 HGNC NCBI

Linked Data

dbSNP Id: rs34782932
MyVariant Identifiers: chr20:g.32304600del (hg19) chr20:g.33716794del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33716794del , CM000682.2:g.33716794del GRCh38
NC_000020.10:g.32304600del , CM000682.1:g.32304600del GRCh37
NC_000020.9:g.31768261del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000409299.8:c.114-2058del MANE Select ENSP00000386385.3:n.114-2058del
ENST00000217398.3:c.114-2058del ENSP00000217398.3:n.114-2058del
ENST00000344022.7:c.114-2058del ENSP00000343071.3:n.114-2058del
ENST00000409299.7:c.114-2058del ENSP00000386385.3:n.114-2058del
NM_007238.4:c.114-2058del NP_009169.3:n.114-2058del
NM_183397.2:c.114-2058del NP_899634.1:n.114-2058del
NM_007238.5:c.114-2058del MANE Select NP_009169.3:n.114-2058del
NM_183397.3:c.114-2058del NP_899634.1:n.114-2058del
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