Canonical Allele Identifier: CA1884222347
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136428866G= , CM000671.2:g.136428866G= GRCh38
NC_000009.11:g.139323318G= , CM000671.1:g.139323318G= GRCh37
NC_000009.10:g.138443139G= NCBI36
NG_016126.1:g.15939C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371712.4:c.*809C= MANE Select ENSP00000360777.3:n.*809C=
ENST00000676019.1:c.*809C= ENSP00000501984.1:n.*809C=
ENST00000371712.3:c.*809C= ENSP00000360777.3:n.*809C=
NM_019892.4:c.*809C= NP_063945.2:n.*809C=
XM_005266094.2:c.*809C= XP_005266151.1:n.*809C=
NM_001318502.1:c.*809C= NP_001305431.1:n.*809C=
NM_019892.5:c.*809C= NP_063945.2:n.*809C=
XM_017014926.1:c.*888C= XP_016870415.1:n.*888C=
NM_019892.6:c.*809C= MANE Select NP_063945.2:n.*809C=
NM_001318502.2:c.*809C= NP_001305431.1:n.*809C=