Canonical Allele Identifier: CA2692606120
Gene: INPP5E HGNC NCBI

Linked Data

gnomAD v4: 9-136428687-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136428687G>C , CM000671.2:g.136428687G>C GRCh38
NC_000009.11:g.139323139G>C , CM000671.1:g.139323139G>C GRCh37
NC_000009.10:g.138442960G>C NCBI36
NG_016126.1:g.16118C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371712.4:c.*988C>G MANE Select ENSP00000360777.3:n.*988C>G
ENST00000676019.1:c.*988C>G ENSP00000501984.1:n.*988C>G
ENST00000371712.3:c.*988C>G ENSP00000360777.3:n.*988C>G
NM_019892.4:c.*988C>G NP_063945.2:n.*988C>G
XM_005266094.2:c.*988C>G XP_005266151.1:n.*988C>G
NM_001318502.1:c.*988C>G NP_001305431.1:n.*988C>G
NM_019892.5:c.*988C>G NP_063945.2:n.*988C>G
XM_017014926.1:c.*1067C>G XP_016870415.1:n.*1067C>G
NM_019892.6:c.*988C>G MANE Select NP_063945.2:n.*988C>G
NM_001318502.2:c.*988C>G NP_001305431.1:n.*988C>G
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