Canonical Allele Identifier: CA292648710
Gene: PPM1E HGNC NCBI

Linked Data

dbSNP Id: rs1016119369
gnomAD v3: 17-58930786-C-T
gnomAD v4: 17-58930786-C-T
MyVariant Identifiers: chr17:g.57008147C>T (hg19) chr17:g.58930786C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58930786C>T , CM000679.2:g.58930786C>T GRCh38
NC_000017.10:g.57008147C>T , CM000679.1:g.57008147C>T GRCh37
NC_000017.9:g.54362929C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000308249.4:c.465-24863C>T MANE Select ENSP00000312411.2:n.465-24863C>T
ENST00000308249.3:c.465-24863C>T ENSP00000312411.2:n.465-24863C>T
NM_014906.4:c.465-24863C>T NP_055721.3:n.465-24863C>T
NR_048561.1:n.594-24863C>T
XM_011524534.1:c.-47-24863C>T XP_011522836.1:n.-47-24863C>T
XM_024450657.1:c.-253-24863C>T XP_024306425.1:n.-253-24863C>T
NM_014906.5:c.465-24863C>T MANE Select NP_055721.3:n.465-24863C>T
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