Canonical Allele Identifier: CA1884222122
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136428654T= , CM000671.2:g.136428654T= GRCh38
NC_000009.11:g.139323106T= , CM000671.1:g.139323106T= GRCh37
NC_000009.10:g.138442927T= NCBI36
NG_016126.1:g.16151A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371712.4:c.*1021A= MANE Select ENSP00000360777.3:n.*1021A=
ENST00000676019.1:c.*1021A= ENSP00000501984.1:n.*1021A=
ENST00000371712.3:c.*1021A= ENSP00000360777.3:n.*1021A=
NM_019892.4:c.*1021A= NP_063945.2:n.*1021A=
XM_005266094.2:c.*1021A= XP_005266151.1:n.*1021A=
NM_001318502.1:c.*1021A= NP_001305431.1:n.*1021A=
NM_019892.5:c.*1021A= NP_063945.2:n.*1021A=
XM_017014926.1:c.*1100A= XP_016870415.1:n.*1100A=
NM_019892.6:c.*1021A= MANE Select NP_063945.2:n.*1021A=
NM_001318502.2:c.*1021A= NP_001305431.1:n.*1021A=