Canonical Allele Identifier: CA3123448568

Gene: PIK3R1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68296299T= , CM000667.2:g.68296299T=	GRCh38
NC_000005.9:g.67592127T= , CM000667.1:g.67592127T=	GRCh37
NC_000005.8:g.67627883T=	NCBI36
NG_012849.2:g.85544T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.1043T=	ENSP00000323512.8:p.Val348=
ENST00000336483.10:c.1133T=	ENSP00000338554.5:p.Val378=
ENST00000517643.2:c.1943T=	ENSP00000513333.1:p.Val648=
ENST00000517698.6:c.*913T=	ENSP00000430424.1:n.*913T=
ENST00000521657.6:c.1943T=	ENSP00000429277.1:p.Val648=
ENST00000522084.6:c.1133T=	ENSP00000429766.2:p.Val378=
ENST00000697457.1:c.1868T=	ENSP00000513315.1:p.Val623=
ENST00000697458.1:c.1943T=	ENSP00000513316.1:p.Val648=
ENST00000697460.1:c.1418T=	ENSP00000513318.1:p.Val473=
ENST00000697461.1:c.1967T=	ENSP00000513319.1:p.Val656=
ENST00000697462.1:c.1157T=	ENSP00000513320.1:p.Val386=
ENST00000697463.1:n.1608T=
ENST00000697464.1:c.*909T=	ENSP00000513322.1:n.*909T=
ENST00000697465.1:c.980T=	ENSP00000513323.1:p.Val327=
ENST00000697466.1:c.950T=	ENSP00000513324.1:p.Val317=
ENST00000697467.1:c.854T=	ENSP00000513325.1:p.Val285=
ENST00000697468.1:c.926T=	ENSP00000513326.1:p.Val309=
ENST00000697469.1:c.635T=	ENSP00000513327.1:p.Val212=
ENST00000697470.1:c.539T=	ENSP00000513328.1:p.Val180=
ENST00000697557.1:c.926T=	ENSP00000513335.1:p.Val309=
ENST00000521381.6:c.1943T= MANE Select	ENSP00000428056.1:p.Val648=
ENST00000320694.12:c.1043T=	ENSP00000323512.8:p.Val348=
ENST00000336483.9:c.1133T=	ENSP00000338554.5:p.Val378=
ENST00000518813.5:n.2486T=
ENST00000521381.5:c.1943T=	ENSP00000428056.1:p.Val648=
ENST00000521657.5:c.1943T=	ENSP00000429277.1:p.Val648=
ENST00000523872.1:c.854T=	ENSP00000430098.1:p.Val285=
NM_001242466.1:c.854T=	NP_001229395.1:p.Val285=
NM_181504.3:c.1133T=	NP_852556.2:p.Val378=
NM_181523.2:c.1943T=	NP_852664.1:p.Val648=
NM_181524.1:c.1043T=	NP_852665.1:p.Val348=
XM_005248542.2:c.1943T=	XP_005248599.1:p.Val648=
XM_011543493.1:c.1616T=	XP_011541795.1:p.Val539=
XM_005248542.3:c.1943T=	XP_005248599.1:p.Val648=
XM_011543493.3:c.1616T=	XP_011541795.1:p.Val539=
XM_017009585.2:c.1943T=	XP_016865074.1:p.Val648=
XM_017009586.1:c.1670T=	XP_016865075.1:p.Val557=
NM_181523.3:c.1943T= MANE Select	NP_852664.1:p.Val648=
NM_001242466.2:c.854T=	NP_001229395.1:p.Val285=
NM_181504.4:c.1133T=	NP_852556.2:p.Val378=
NM_181524.2:c.1043T=	NP_852665.1:p.Val348=