Canonical Allele Identifier: CA1553404853

Gene: PIK3R1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.78G=	ENSP00000323512.8:p.Met26=
ENST00000336483.10:c.168G=	ENSP00000338554.5:p.Met56=
ENST00000517643.2:c.978G=	ENSP00000513333.1:p.Met326=
ENST00000517698.6:c.107-781G=	ENSP00000430424.1:n.107-781G=
ENST00000521657.6:c.978G=	ENSP00000429277.1:p.Met326=
ENST00000522084.6:c.168G=	ENSP00000429766.2:p.Met56=
ENST00000697457.1:c.903G=	ENSP00000513315.1:p.Met301=
ENST00000697458.1:c.978G=	ENSP00000513316.1:p.Met326=
ENST00000697460.1:c.453G=	ENSP00000513318.1:p.Met151=
ENST00000697461.1:c.978G=	ENSP00000513319.1:p.Met326=
ENST00000697462.1:c.168G=	ENSP00000513320.1:p.Met56=
ENST00000697464.1:c.168G=	ENSP00000513322.1:p.Met56=
ENST00000697465.1:c.15G=	ENSP00000513323.1:p.Met5=
ENST00000697466.1:c.-11G=	ENSP00000513324.1:n.-11G=
ENST00000697556.1:c.885G=	ENSP00000513334.1:p.Met295=
ENST00000521381.6:c.978G= MANE Select	ENSP00000428056.1:p.Met326=
ENST00000320694.12:c.78G=	ENSP00000323512.8:p.Met26=
ENST00000336483.9:c.168G=	ENSP00000338554.5:p.Met56=
ENST00000517698.5:c.107-781G=	ENSP00000430424.1:n.107-781G=
ENST00000518292.1:n.225G=
ENST00000518813.5:n.1521G=
ENST00000521381.5:c.978G=	ENSP00000428056.1:p.Met326=
ENST00000521409.5:c.-70-781G=	ENSP00000431058.1:n.-70-781G=
ENST00000521657.5:c.978G=	ENSP00000429277.1:p.Met326=
ENST00000522084.5:c.168G=	ENSP00000429766.1:p.Met56=
ENST00000523807.5:c.168G=	ENSP00000430126.1:p.Met56=
NM_181504.3:c.168G=	NP_852556.2:p.Met56=
NM_181523.2:c.978G=	NP_852664.1:p.Met326=
NM_181524.1:c.78G=	NP_852665.1:p.Met26=
XM_005248542.2:c.978G=	XP_005248599.1:p.Met326=
XM_011543493.1:c.651G=	XP_011541795.1:p.Met217=
XM_005248542.3:c.978G=	XP_005248599.1:p.Met326=
XM_011543493.3:c.651G=	XP_011541795.1:p.Met217=
XM_017009585.2:c.978G=	XP_016865074.1:p.Met326=
XM_017009586.1:c.705G=	XP_016865075.1:p.Met235=
NM_181523.3:c.978G= MANE Select	NP_852664.1:p.Met326=
NM_181504.4:c.168G=	NP_852556.2:p.Met56=
NM_181524.2:c.78G=	NP_852665.1:p.Met26=