Canonical Allele Identifier: CA359878374

Gene: PIK3R1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68292320G>T , CM000667.2:g.68292320G>T	GRCh38
NC_000005.9:g.67588148G>T , CM000667.1:g.67588148G>T	GRCh37
NC_000005.8:g.67623904G>T	NCBI36
NG_012849.2:g.81565G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.78G>T	ENSP00000323512.8:p.Met26Ile
ENST00000336483.10:c.168G>T	ENSP00000338554.5:p.Met56Ile
ENST00000517643.2:c.978G>T	ENSP00000513333.1:p.Met326Ile
ENST00000517698.6:c.107-781G>T	ENSP00000430424.1:n.107-781G>T
ENST00000521657.6:c.978G>T	ENSP00000429277.1:p.Met326Ile
ENST00000522084.6:c.168G>T	ENSP00000429766.2:p.Met56Ile
ENST00000697457.1:c.903G>T	ENSP00000513315.1:p.Met301Ile
ENST00000697458.1:c.978G>T	ENSP00000513316.1:p.Met326Ile
ENST00000697460.1:c.453G>T	ENSP00000513318.1:p.Met151Ile
ENST00000697461.1:c.978G>T	ENSP00000513319.1:p.Met326Ile
ENST00000697462.1:c.168G>T	ENSP00000513320.1:p.Met56Ile
ENST00000697464.1:c.168G>T	ENSP00000513322.1:p.Met56Ile
ENST00000697465.1:c.15G>T	ENSP00000513323.1:p.Met5Ile
ENST00000697466.1:c.-11G>T	ENSP00000513324.1:n.-11G>T
ENST00000697556.1:c.885G>T	ENSP00000513334.1:p.Met295Ile
ENST00000521381.6:c.978G>T MANE Select	ENSP00000428056.1:p.Met326Ile
ENST00000320694.12:c.78G>T	ENSP00000323512.8:p.Met26Ile
ENST00000336483.9:c.168G>T	ENSP00000338554.5:p.Met56Ile
ENST00000517698.5:c.107-781G>T	ENSP00000430424.1:n.107-781G>T
ENST00000518292.1:n.225G>T
ENST00000518813.5:n.1521G>T
ENST00000521381.5:c.978G>T	ENSP00000428056.1:p.Met326Ile
ENST00000521409.5:c.-70-781G>T	ENSP00000431058.1:n.-70-781G>T
ENST00000521657.5:c.978G>T	ENSP00000429277.1:p.Met326Ile
ENST00000522084.5:c.168G>T	ENSP00000429766.1:p.Met56Ile
ENST00000523807.5:c.168G>T	ENSP00000430126.1:p.Met56Ile
NM_181504.3:c.168G>T	NP_852556.2:p.Met56Ile
NM_181523.2:c.978G>T	NP_852664.1:p.Met326Ile
NM_181524.1:c.78G>T	NP_852665.1:p.Met26Ile
XM_005248542.2:c.978G>T	XP_005248599.1:p.Met326Ile
XM_011543493.1:c.651G>T	XP_011541795.1:p.Met217Ile
XM_005248542.3:c.978G>T	XP_005248599.1:p.Met326Ile
XM_011543493.3:c.651G>T	XP_011541795.1:p.Met217Ile
XM_017009585.2:c.978G>T	XP_016865074.1:p.Met326Ile
XM_017009586.1:c.705G>T	XP_016865075.1:p.Met235Ile
NM_181523.3:c.978G>T MANE Select	NP_852664.1:p.Met326Ile
NM_181504.4:c.168G>T	NP_852556.2:p.Met56Ile
NM_181524.2:c.78G>T	NP_852665.1:p.Met26Ile