Canonical Allele Identifier: CA1884222232

Gene: INPP5E

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136428768C= , CM000671.2:g.136428768C=	GRCh38
NC_000009.11:g.139323220C= , CM000671.1:g.139323220C=	GRCh37
NC_000009.10:g.138443041C=	NCBI36
NG_016126.1:g.16037G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371712.4:c.*907G= MANE Select	ENSP00000360777.3:n.*907G=
ENST00000676019.1:c.*907G=	ENSP00000501984.1:n.*907G=
ENST00000371712.3:c.*907G=	ENSP00000360777.3:n.*907G=
NM_019892.4:c.*907G=	NP_063945.2:n.*907G=
XM_005266094.2:c.*907G=	XP_005266151.1:n.*907G=
NM_001318502.1:c.*907G=	NP_001305431.1:n.*907G=
NM_019892.5:c.*907G=	NP_063945.2:n.*907G=
XM_017014926.1:c.*986G=	XP_016870415.1:n.*986G=
NM_019892.6:c.*907G= MANE Select	NP_063945.2:n.*907G=
NM_001318502.2:c.*907G=	NP_001305431.1:n.*907G=