Canonical Allele Identifier: CA15406386

Gene: PIK3R1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68274310G>A , CM000667.2:g.68274310G>A	GRCh38
NC_000005.9:g.67570138G>A , CM000667.1:g.67570138G>A	GRCh37
NC_000005.8:g.67605894G>A	NCBI36
NG_012849.2:g.63555G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517412.2:n.1855G>A
ENST00000517643.2:c.502+297G>A	ENSP00000513333.1:n.502+297G>A
ENST00000521657.6:c.502+297G>A	ENSP00000429277.1:n.502+297G>A
ENST00000697457.1:c.427+828G>A	ENSP00000513315.1:n.427+828G>A
ENST00000697458.1:c.502+297G>A	ENSP00000513316.1:n.502+297G>A
ENST00000697460.1:c.-24+297G>A	ENSP00000513318.1:n.-24+297G>A
ENST00000697461.1:c.502+297G>A	ENSP00000513319.1:n.502+297G>A
ENST00000697556.1:c.409+297G>A	ENSP00000513334.1:n.409+297G>A
ENST00000521381.6:c.502+297G>A MANE Select	ENSP00000428056.1:n.502+297G>A
ENST00000520675.1:c.208+297G>A	ENSP00000428566.1:n.208+297G>A
ENST00000521381.5:c.502+297G>A	ENSP00000428056.1:n.502+297G>A
ENST00000521657.5:c.502+297G>A	ENSP00000429277.1:n.502+297G>A
NM_181523.2:c.502+297G>A	NP_852664.1:n.502+297G>A
XM_005248542.2:c.502+297G>A	XP_005248599.1:n.502+297G>A
XM_011543493.1:c.175+297G>A	XP_011541795.1:n.175+297G>A
XM_005248542.3:c.502+297G>A	XP_005248599.1:n.502+297G>A
XM_011543493.3:c.175+297G>A	XP_011541795.1:n.175+297G>A
XM_017009585.2:c.502+297G>A	XP_016865074.1:n.502+297G>A
XM_017009586.1:c.229+297G>A	XP_016865075.1:n.229+297G>A
NM_181523.3:c.502+297G>A MANE Select	NP_852664.1:n.502+297G>A