Canonical Allele Identifier: CA2692606106

Gene: INPP5E

Linked Data

• gnomAD v4: 9-136428671-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136428671T>A , CM000671.2:g.136428671T>A	GRCh38
NC_000009.11:g.139323123T>A , CM000671.1:g.139323123T>A	GRCh37
NC_000009.10:g.138442944T>A	NCBI36
NG_016126.1:g.16134A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371712.4:c.*1004A>T MANE Select	ENSP00000360777.3:n.*1004A>T
ENST00000676019.1:c.*1004A>T	ENSP00000501984.1:n.*1004A>T
ENST00000371712.3:c.*1004A>T	ENSP00000360777.3:n.*1004A>T
NM_019892.4:c.*1004A>T	NP_063945.2:n.*1004A>T
XM_005266094.2:c.*1004A>T	XP_005266151.1:n.*1004A>T
NM_001318502.1:c.*1004A>T	NP_001305431.1:n.*1004A>T
NM_019892.5:c.*1004A>T	NP_063945.2:n.*1004A>T
XM_017014926.1:c.*1083A>T	XP_016870415.1:n.*1083A>T
NM_019892.6:c.*1004A>T MANE Select	NP_063945.2:n.*1004A>T
NM_001318502.2:c.*1004A>T	NP_001305431.1:n.*1004A>T