Canonical Allele Identifier: CA2580899823
Gene: INPP5E HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136428749A>T , CM000671.2:g.136428749A>T GRCh38
NC_000009.11:g.139323201A>T , CM000671.1:g.139323201A>T GRCh37
NC_000009.10:g.138443022A>T NCBI36
NG_016126.1:g.16056T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371712.4:c.*926T>A MANE Select ENSP00000360777.3:n.*926T>A
ENST00000676019.1:c.*926T>A ENSP00000501984.1:n.*926T>A
ENST00000371712.3:c.*926T>A ENSP00000360777.3:n.*926T>A
NM_019892.4:c.*926T>A NP_063945.2:n.*926T>A
XM_005266094.2:c.*926T>A XP_005266151.1:n.*926T>A
NM_001318502.1:c.*926T>A NP_001305431.1:n.*926T>A
NM_019892.5:c.*926T>A NP_063945.2:n.*926T>A
XM_017014926.1:c.*1005T>A XP_016870415.1:n.*1005T>A
NM_019892.6:c.*926T>A MANE Select NP_063945.2:n.*926T>A
NM_001318502.2:c.*926T>A NP_001305431.1:n.*926T>A
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