Canonical Allele Identifier: CA1884222229

Gene: INPP5E

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136428765G= , CM000671.2:g.136428765G=	GRCh38
NC_000009.11:g.139323217G= , CM000671.1:g.139323217G=	GRCh37
NC_000009.10:g.138443038G=	NCBI36
NG_016126.1:g.16040C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371712.4:c.*910C= MANE Select	ENSP00000360777.3:n.*910C=
ENST00000676019.1:c.*910C=	ENSP00000501984.1:n.*910C=
ENST00000371712.3:c.*910C=	ENSP00000360777.3:n.*910C=
NM_019892.4:c.*910C=	NP_063945.2:n.*910C=
XM_005266094.2:c.*910C=	XP_005266151.1:n.*910C=
NM_001318502.1:c.*910C=	NP_001305431.1:n.*910C=
NM_019892.5:c.*910C=	NP_063945.2:n.*910C=
XM_017014926.1:c.*989C=	XP_016870415.1:n.*989C=
NM_019892.6:c.*910C= MANE Select	NP_063945.2:n.*910C=
NM_001318502.2:c.*910C=	NP_001305431.1:n.*910C=