Canonical Allele Identifier: CA1553387911

Gene: PIK3R1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68252569_68252573delinsGTGCT , CM000667.2:g.68252569_68252573delinsGTGCT	GRCh38
NC_000005.9:g.67548397_67548401delinsGTGCT , CM000667.1:g.67548397_67548401delinsGTGCT	GRCh37
NC_000005.8:g.67584153_67584157delinsGTGCT	NCBI36
NG_012849.2:g.41814_41818delinsGTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517412.2:n.935-20821_935-20817delinsGTGCT
ENST00000517643.2:c.335-20821_335-20817delinsGTGCT	ENSP00000513333.1:n.335-20821_335-20817delinsGTGCT
ENST00000521657.6:c.335-20821_335-20817delinsGTGCT	ENSP00000429277.1:n.335-20821_335-20817delinsGTGCT
ENST00000697457.1:c.335-20821_335-20817delinsGTGCT	ENSP00000513315.1:n.335-20821_335-20817delinsGTGCT
ENST00000697458.1:c.335-20821_335-20817delinsGTGCT	ENSP00000513316.1:n.335-20821_335-20817delinsGTGCT
ENST00000697460.1:c.-191-20821_-191-20817delinsGTGCT	ENSP00000513318.1:n.-191-20821_-191-20817delinsGTGCT
ENST00000697461.1:c.335-20821_335-20817delinsGTGCT	ENSP00000513319.1:n.335-20821_335-20817delinsGTGCT
ENST00000697556.1:c.335-21370_335-21366delinsGTGCT	ENSP00000513334.1:n.335-21370_335-21366delinsGTGCT
ENST00000521381.6:c.335-20821_335-20817delinsGTGCT MANE Select	ENSP00000428056.1:n.335-20821_335-20817delinsGTGCT
ENST00000517412.1:n.574-20821_574-20817delinsGTGCT
ENST00000520675.1:c.40+12632_40+12636delinsGTGCT	ENSP00000428566.1:n.40+12632_40+12636delinsGTGCT
ENST00000521381.5:c.335-20821_335-20817delinsGTGCT	ENSP00000428056.1:n.335-20821_335-20817delinsGTGCT
ENST00000521657.5:c.335-20821_335-20817delinsGTGCT	ENSP00000429277.1:n.335-20821_335-20817delinsGTGCT
NM_181523.2:c.335-20821_335-20817delinsGTGCT	NP_852664.1:n.335-20821_335-20817delinsGTGCT
XM_005248542.2:c.335-20821_335-20817delinsGTGCT	XP_005248599.1:n.335-20821_335-20817delinsGTGCT
XM_011543493.1:c.7+311_7+315delinsGTGCT	XP_011541795.1:n.7+311_7+315delinsGTGCT
XM_005248542.3:c.335-20821_335-20817delinsGTGCT	XP_005248599.1:n.335-20821_335-20817delinsGTGCT
XM_011543493.3:c.7+311_7+315delinsGTGCT	XP_011541795.1:n.7+311_7+315delinsGTGCT
XM_017009585.2:c.335-20821_335-20817delinsGTGCT	XP_016865074.1:n.335-20821_335-20817delinsGTGCT
XM_017009586.1:c.61+12632_61+12636delinsGTGCT	XP_016865075.1:n.61+12632_61+12636delinsGTGCT
NM_181523.3:c.335-20821_335-20817delinsGTGCT MANE Select	NP_852664.1:n.335-20821_335-20817delinsGTGCT