Canonical Allele Identifier: CA1884224140

Gene: INPP5E

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136430300C= , CM000671.2:g.136430300C=	GRCh38
NC_000009.11:g.139324752C= , CM000671.1:g.139324752C=	GRCh37
NC_000009.10:g.138444573C=	NCBI36
NG_016126.1:g.14505G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371712.4:c.1779G= MANE Select	ENSP00000360777.3:p.Val593=
ENST00000676019.1:c.1677G=	ENSP00000501984.1:p.Val559=
ENST00000371712.3:c.1779G=	ENSP00000360777.3:p.Val593=
NM_019892.4:c.1779G=	NP_063945.2:p.Val593=
XM_005266094.2:c.1776G=	XP_005266151.1:p.Val592=
NM_001318502.1:c.1776G=	NP_001305431.1:p.Val592=
NM_019892.5:c.1779G=	NP_063945.2:p.Val593=
XM_017014926.1:c.1779G=	XP_016870415.1:p.Val593=
XR_929828.2:n.2384G=
NM_019892.6:c.1779G= MANE Select	NP_063945.2:p.Val593=
NM_001318502.2:c.1776G=	NP_001305431.1:p.Val592=