Canonical Allele Identifier: CA653614430
Gene: INPP5E HGNC NCBI

Linked Data

COSMIC: COSN2312968 COSN2312969
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136428703T>G , CM000671.2:g.136428703T>G GRCh38
NC_000009.11:g.139323155T>G , CM000671.1:g.139323155T>G GRCh37
NC_000009.10:g.138442976T>G NCBI36
NG_016126.1:g.16102A>C

Transcript Alleles

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