Canonical Allele Identifier: CA2692606117

Gene: INPP5E

Linked Data

• gnomAD v4: 9-136428686-TG-T

Genomic Alleles

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

Transcript Alleles

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