Canonical Allele Identifier: CA1553387961

Gene: PIK3R1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68252617_68252618delinsAT , CM000667.2:g.68252617_68252618delinsAT	GRCh38
NC_000005.9:g.67548445_67548446delinsAT , CM000667.1:g.67548445_67548446delinsAT	GRCh37
NC_000005.8:g.67584201_67584202delinsAT	NCBI36
NG_012849.2:g.41862_41863delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517412.2:n.935-20773_935-20772delinsAT
ENST00000517643.2:c.335-20773_335-20772delinsAT	ENSP00000513333.1:n.335-20773_335-20772delinsAT
ENST00000521657.6:c.335-20773_335-20772delinsAT	ENSP00000429277.1:n.335-20773_335-20772delinsAT
ENST00000697457.1:c.335-20773_335-20772delinsAT	ENSP00000513315.1:n.335-20773_335-20772delinsAT
ENST00000697458.1:c.335-20773_335-20772delinsAT	ENSP00000513316.1:n.335-20773_335-20772delinsAT
ENST00000697460.1:c.-191-20773_-191-20772delinsAT	ENSP00000513318.1:n.-191-20773_-191-20772delinsAT
ENST00000697461.1:c.335-20773_335-20772delinsAT	ENSP00000513319.1:n.335-20773_335-20772delinsAT
ENST00000697556.1:c.335-21322_335-21321delinsAT	ENSP00000513334.1:n.335-21322_335-21321delinsAT
ENST00000521381.6:c.335-20773_335-20772delinsAT MANE Select	ENSP00000428056.1:n.335-20773_335-20772delinsAT
ENST00000517412.1:n.574-20773_574-20772delinsAT
ENST00000520675.1:c.40+12680_40+12681delinsAT	ENSP00000428566.1:n.40+12680_40+12681delinsAT
ENST00000521381.5:c.335-20773_335-20772delinsAT	ENSP00000428056.1:n.335-20773_335-20772delinsAT
ENST00000521657.5:c.335-20773_335-20772delinsAT	ENSP00000429277.1:n.335-20773_335-20772delinsAT
NM_181523.2:c.335-20773_335-20772delinsAT	NP_852664.1:n.335-20773_335-20772delinsAT
XM_005248542.2:c.335-20773_335-20772delinsAT	XP_005248599.1:n.335-20773_335-20772delinsAT
XM_011543493.1:c.7+359_7+360delinsAT	XP_011541795.1:n.7+359_7+360delinsAT
XM_005248542.3:c.335-20773_335-20772delinsAT	XP_005248599.1:n.335-20773_335-20772delinsAT
XM_011543493.3:c.7+359_7+360delinsAT	XP_011541795.1:n.7+359_7+360delinsAT
XM_017009585.2:c.335-20773_335-20772delinsAT	XP_016865074.1:n.335-20773_335-20772delinsAT
XM_017009586.1:c.61+12680_61+12681delinsAT	XP_016865075.1:n.61+12680_61+12681delinsAT
NM_181523.3:c.335-20773_335-20772delinsAT MANE Select	NP_852664.1:n.335-20773_335-20772delinsAT