Canonical Allele Identifier: CA1884222228
Gene: INPP5E HGNC NCBI

Linked Data

dbSNP Id: rs1835630506

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136428765_136428769del , CM000671.2:g.136428765_136428769del GRCh38
NC_000009.11:g.139323217_139323221del , CM000671.1:g.139323217_139323221del GRCh37
NC_000009.10:g.138443038_138443042del NCBI36
NG_016126.1:g.16036_16040del

Transcript Alleles

HGVS Amino-acid change
ENST00000371712.4:c.*906_*910del MANE Select ENSP00000360777.3:n.*906_*910del
ENST00000676019.1:c.*906_*910del ENSP00000501984.1:n.*906_*910del
ENST00000371712.3:c.*906_*910del ENSP00000360777.3:n.*906_*910del
NM_019892.4:c.*906_*910del NP_063945.2:n.*906_*910del
XM_005266094.2:c.*906_*910del XP_005266151.1:n.*906_*910del
NM_001318502.1:c.*906_*910del NP_001305431.1:n.*906_*910del
NM_019892.5:c.*906_*910del NP_063945.2:n.*906_*910del
XM_017014926.1:c.*985_*989del XP_016870415.1:n.*985_*989del
NM_019892.6:c.*906_*910del MANE Select NP_063945.2:n.*906_*910del
NM_001318502.2:c.*906_*910del NP_001305431.1:n.*906_*910del