Canonical Allele Identifier: CA1553387647

Gene: PIK3R1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68252337_68252338delinsAG , CM000667.2:g.68252337_68252338delinsAG	GRCh38
NC_000005.9:g.67548165_67548166delinsAG , CM000667.1:g.67548165_67548166delinsAG	GRCh37
NC_000005.8:g.67583921_67583922delinsAG	NCBI36
NG_012849.2:g.41582_41583delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517412.2:n.935-21053_935-21052delinsAG
ENST00000517643.2:c.335-21053_335-21052delinsAG	ENSP00000513333.1:n.335-21053_335-21052delinsAG
ENST00000521657.6:c.335-21053_335-21052delinsAG	ENSP00000429277.1:n.335-21053_335-21052delinsAG
ENST00000697457.1:c.335-21053_335-21052delinsAG	ENSP00000513315.1:n.335-21053_335-21052delinsAG
ENST00000697458.1:c.335-21053_335-21052delinsAG	ENSP00000513316.1:n.335-21053_335-21052delinsAG
ENST00000697460.1:c.-191-21053_-191-21052delinsAG	ENSP00000513318.1:n.-191-21053_-191-21052delinsAG
ENST00000697461.1:c.335-21053_335-21052delinsAG	ENSP00000513319.1:n.335-21053_335-21052delinsAG
ENST00000697556.1:c.335-21602_335-21601delinsAG	ENSP00000513334.1:n.335-21602_335-21601delinsAG
ENST00000521381.6:c.335-21053_335-21052delinsAG MANE Select	ENSP00000428056.1:n.335-21053_335-21052delinsAG
ENST00000517412.1:n.574-21053_574-21052delinsAG
ENST00000520675.1:c.40+12400_40+12401delinsAG	ENSP00000428566.1:n.40+12400_40+12401delinsAG
ENST00000521381.5:c.335-21053_335-21052delinsAG	ENSP00000428056.1:n.335-21053_335-21052delinsAG
ENST00000521657.5:c.335-21053_335-21052delinsAG	ENSP00000429277.1:n.335-21053_335-21052delinsAG
NM_181523.2:c.335-21053_335-21052delinsAG	NP_852664.1:n.335-21053_335-21052delinsAG
XM_005248542.2:c.335-21053_335-21052delinsAG	XP_005248599.1:n.335-21053_335-21052delinsAG
XM_011543493.1:c.7+79_7+80delinsAG	XP_011541795.1:n.7+79_7+80delinsAG
XM_005248542.3:c.335-21053_335-21052delinsAG	XP_005248599.1:n.335-21053_335-21052delinsAG
XM_011543493.3:c.7+79_7+80delinsAG	XP_011541795.1:n.7+79_7+80delinsAG
XM_017009585.2:c.335-21053_335-21052delinsAG	XP_016865074.1:n.335-21053_335-21052delinsAG
XM_017009586.1:c.61+12400_61+12401delinsAG	XP_016865075.1:n.61+12400_61+12401delinsAG
NM_181523.3:c.335-21053_335-21052delinsAG MANE Select	NP_852664.1:n.335-21053_335-21052delinsAG