Canonical Allele Identifier: CA1884222131

Gene: INPP5E

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136428667_136428672delinsATAATT , CM000671.2:g.136428667_136428672delinsATAATT	GRCh38
NC_000009.11:g.139323119_139323124delinsATAATT , CM000671.1:g.139323119_139323124delinsATAATT	GRCh37
NC_000009.10:g.138442940_138442945delinsATAATT	NCBI36
NG_016126.1:g.16133_16138delinsAATTAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000371712.4:c.*1003_*1008delinsAATTAT MANE Select	ENSP00000360777.3:n.*1003_*1008delinsAATT...
ENST00000676019.1:c.*1003_*1008delinsAATTAT	ENSP00000501984.1:n.*1003_*1008delinsAATT...
ENST00000371712.3:c.*1003_*1008delinsAATTAT	ENSP00000360777.3:n.*1003_*1008delinsAATT...
NM_019892.4:c.*1003_*1008delinsAATTAT	NP_063945.2:n.*1003_*1008delinsAATTAT
XM_005266094.2:c.*1003_*1008delinsAATTAT	XP_005266151.1:n.*1003_*1008delinsAATTAT
NM_001318502.1:c.*1003_*1008delinsAATTAT	NP_001305431.1:n.*1003_*1008delinsAATTAT
NM_019892.5:c.*1003_*1008delinsAATTAT	NP_063945.2:n.*1003_*1008delinsAATTAT
XM_017014926.1:c.*1082_*1087delinsAATTAT	XP_016870415.1:n.*1082_*1087delinsAATTAT
NM_019892.6:c.*1003_*1008delinsAATTAT MANE Select	NP_063945.2:n.*1003_*1008delinsAATTAT
NM_001318502.2:c.*1003_*1008delinsAATTAT	NP_001305431.1:n.*1003_*1008delinsAATTAT