Canonical Allele Identifier: CA1884222164

Gene: INPP5E

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136428696T= , CM000671.2:g.136428696T=	GRCh38
NC_000009.11:g.139323148T= , CM000671.1:g.139323148T=	GRCh37
NC_000009.10:g.138442969T=	NCBI36
NG_016126.1:g.16109A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371712.4:c.*979A= MANE Select	ENSP00000360777.3:n.*979A=
ENST00000676019.1:c.*979A=	ENSP00000501984.1:n.*979A=
ENST00000371712.3:c.*979A=	ENSP00000360777.3:n.*979A=
NM_019892.4:c.*979A=	NP_063945.2:n.*979A=
XM_005266094.2:c.*979A=	XP_005266151.1:n.*979A=
NM_001318502.1:c.*979A=	NP_001305431.1:n.*979A=
NM_019892.5:c.*979A=	NP_063945.2:n.*979A=
XM_017014926.1:c.*1058A=	XP_016870415.1:n.*1058A=
NM_019892.6:c.*979A= MANE Select	NP_063945.2:n.*979A=
NM_001318502.2:c.*979A=	NP_001305431.1:n.*979A=