Canonical Allele Identifier: CA1553387713

Gene: PIK3R1

Linked Data

• dbSNP Id: rs1745348094

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68252373_68252374insC , CM000667.2:g.68252373_68252374insC	GRCh38
NC_000005.9:g.67548201_67548202insC , CM000667.1:g.67548201_67548202insC	GRCh37
NC_000005.8:g.67583957_67583958insC	NCBI36
NG_012849.2:g.41618_41619insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517412.2:n.935-21017_935-21016insC
ENST00000517643.2:c.335-21017_335-21016insC	ENSP00000513333.1:n.335-21017_335-21016insC
ENST00000521657.6:c.335-21017_335-21016insC	ENSP00000429277.1:n.335-21017_335-21016insC
ENST00000697457.1:c.335-21017_335-21016insC	ENSP00000513315.1:n.335-21017_335-21016insC
ENST00000697458.1:c.335-21017_335-21016insC	ENSP00000513316.1:n.335-21017_335-21016insC
ENST00000697460.1:c.-191-21017_-191-21016insC	ENSP00000513318.1:n.-191-21017_-191-21016insC
ENST00000697461.1:c.335-21017_335-21016insC	ENSP00000513319.1:n.335-21017_335-21016insC
ENST00000697556.1:c.335-21566_335-21565insC	ENSP00000513334.1:n.335-21566_335-21565insC
ENST00000521381.6:c.335-21017_335-21016insC MANE Select	ENSP00000428056.1:n.335-21017_335-21016insC
ENST00000517412.1:n.574-21017_574-21016insC
ENST00000520675.1:c.40+12436_40+12437insC	ENSP00000428566.1:n.40+12436_40+12437insC
ENST00000521381.5:c.335-21017_335-21016insC	ENSP00000428056.1:n.335-21017_335-21016insC
ENST00000521657.5:c.335-21017_335-21016insC	ENSP00000429277.1:n.335-21017_335-21016insC
NM_181523.2:c.335-21017_335-21016insC	NP_852664.1:n.335-21017_335-21016insC
XM_005248542.2:c.335-21017_335-21016insC	XP_005248599.1:n.335-21017_335-21016insC
XM_011543493.1:c.7+115_7+116insC	XP_011541795.1:n.7+115_7+116insC
XM_005248542.3:c.335-21017_335-21016insC	XP_005248599.1:n.335-21017_335-21016insC
XM_011543493.3:c.7+115_7+116insC	XP_011541795.1:n.7+115_7+116insC
XM_017009585.2:c.335-21017_335-21016insC	XP_016865074.1:n.335-21017_335-21016insC
XM_017009586.1:c.61+12436_61+12437insC	XP_016865075.1:n.61+12436_61+12437insC
NM_181523.3:c.335-21017_335-21016insC MANE Select	NP_852664.1:n.335-21017_335-21016insC