Canonical Allele Identifier: CA1884222166
Gene: INPP5E HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136428703_136428705delinsTCA , CM000671.2:g.136428703_136428705delinsTCA GRCh38
NC_000009.11:g.139323155_139323157delinsTCA , CM000671.1:g.139323155_139323157delinsTCA GRCh37
NC_000009.10:g.138442976_138442978delinsTCA NCBI36
NG_016126.1:g.16100_16102delinsTGA

Transcript Alleles

HGVS Amino-acid change
ENST00000371712.4:c.*970_*972delinsTGA MANE Select ENSP00000360777.3:n.*970_*972delinsTGA
ENST00000676019.1:c.*970_*972delinsTGA ENSP00000501984.1:n.*970_*972delinsTGA
ENST00000371712.3:c.*970_*972delinsTGA ENSP00000360777.3:n.*970_*972delinsTGA
NM_019892.4:c.*970_*972delinsTGA NP_063945.2:n.*970_*972delinsTGA
XM_005266094.2:c.*970_*972delinsTGA XP_005266151.1:n.*970_*972delinsTGA
NM_001318502.1:c.*970_*972delinsTGA NP_001305431.1:n.*970_*972delinsTGA
NM_019892.5:c.*970_*972delinsTGA NP_063945.2:n.*970_*972delinsTGA
XM_017014926.1:c.*1049_*1051delinsTGA XP_016870415.1:n.*1049_*1051delinsTGA
NM_019892.6:c.*970_*972delinsTGA MANE Select NP_063945.2:n.*970_*972delinsTGA
NM_001318502.2:c.*970_*972delinsTGA NP_001305431.1:n.*970_*972delinsTGA
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