Canonical Allele Identifier: CA1884225530

Gene: INPP5E

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136432505T= , CM000671.2:g.136432505T=	GRCh38
NC_000009.11:g.139326957T= , CM000671.1:g.139326957T=	GRCh37
NC_000009.10:g.138446778T=	NCBI36
NG_016126.1:g.12300A=

Transcript Alleles

HGVS	Amino-acid Change
NM_019892.6:c.1361A= MANE Select	NP_063945.2:p.Asp454=
ENST00000371712.4:c.1361A= MANE Select	ENSP00000360777.3:p.Asp454=
NM_001318502.1:c.1358A=	NP_001305431.1:p.Asp453=
NM_001318502.2:c.1358A=	NP_001305431.1:p.Asp453=
NM_019892.4:c.1361A=	NP_063945.2:p.Asp454=
NM_019892.5:c.1361A=	NP_063945.2:p.Asp454=
ENST00000371712.3:c.1361A=	ENSP00000360777.3:p.Asp454=
ENST00000676019.1:c.1259A=	ENSP00000501984.1:p.Asp420=
XM_005266094.2:c.1358A=	XP_005266151.1:p.Asp453=
XM_017014926.1:c.1361A=	XP_016870415.1:p.Asp454=
XR_929828.1:n.1801A=
XR_929828.2:n.1803A=