Canonical Allele Identifier: CA444672540

Gene: PIK3R1

Linked Data

• MyVariant Identifiers: chr5:g.67591006T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295178T>G , CM000667.2:g.68295178T>G	GRCh38
NC_000005.9:g.67591006T>G , CM000667.1:g.67591006T>G	GRCh37
NC_000005.8:g.67626762T>G	NCBI36
NG_012849.2:g.84423T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.699T>G	ENSP00000323512.8:p.Ser233=
ENST00000336483.10:c.789T>G	ENSP00000338554.5:p.Ser263=
ENST00000517643.2:c.1599T>G	ENSP00000513333.1:p.Ser533=
ENST00000517698.6:c.*569T>G	ENSP00000430424.1:n.*569T>G
ENST00000521657.6:c.1599T>G	ENSP00000429277.1:p.Ser533=
ENST00000522084.6:c.789T>G	ENSP00000429766.2:p.Ser263=
ENST00000697457.1:c.1524T>G	ENSP00000513315.1:p.Ser508=
ENST00000697458.1:c.1599T>G	ENSP00000513316.1:p.Ser533=
ENST00000697460.1:c.1074T>G	ENSP00000513318.1:p.Ser358=
ENST00000697461.1:c.1599T>G	ENSP00000513319.1:p.Ser533=
ENST00000697462.1:c.789T>G	ENSP00000513320.1:p.Ser263=
ENST00000697463.1:n.1240T>G
ENST00000697464.1:c.*565T>G	ENSP00000513322.1:n.*565T>G
ENST00000697465.1:c.636T>G	ENSP00000513323.1:p.Ser212=
ENST00000697466.1:c.606T>G	ENSP00000513324.1:p.Ser202=
ENST00000697467.1:c.510T>G	ENSP00000513325.1:p.Ser170=
ENST00000697468.1:c.582T>G	ENSP00000513326.1:p.Ser194=
ENST00000697469.1:c.291T>G	ENSP00000513327.1:p.Ser97=
ENST00000697470.1:c.195T>G	ENSP00000513328.1:p.Ser65=
ENST00000697557.1:c.582T>G	ENSP00000513335.1:p.Ser194=
ENST00000521381.6:c.1599T>G MANE Select	ENSP00000428056.1:p.Ser533=
ENST00000320694.12:c.699T>G	ENSP00000323512.8:p.Ser233=
ENST00000336483.9:c.789T>G	ENSP00000338554.5:p.Ser263=
ENST00000517698.5:c.*569T>G	ENSP00000430424.1:n.*569T>G
ENST00000518813.5:n.2142T>G
ENST00000520550.1:n.998T>G
ENST00000521381.5:c.1599T>G	ENSP00000428056.1:p.Ser533=
ENST00000521657.5:c.1599T>G	ENSP00000429277.1:p.Ser533=
ENST00000523872.1:c.510T>G	ENSP00000430098.1:p.Ser170=
NM_001242466.1:c.510T>G	NP_001229395.1:p.Ser170=
NM_181504.3:c.789T>G	NP_852556.2:p.Ser263=
NM_181523.2:c.1599T>G	NP_852664.1:p.Ser533=
NM_181524.1:c.699T>G	NP_852665.1:p.Ser233=
XM_005248542.2:c.1599T>G	XP_005248599.1:p.Ser533=
XM_011543493.1:c.1272T>G	XP_011541795.1:p.Ser424=
XM_005248542.3:c.1599T>G	XP_005248599.1:p.Ser533=
XM_011543493.3:c.1272T>G	XP_011541795.1:p.Ser424=
XM_017009585.2:c.1599T>G	XP_016865074.1:p.Ser533=
XM_017009586.1:c.1326T>G	XP_016865075.1:p.Ser442=
NM_181523.3:c.1599T>G MANE Select	NP_852664.1:p.Ser533=
NM_001242466.2:c.510T>G	NP_001229395.1:p.Ser170=
NM_181504.4:c.789T>G	NP_852556.2:p.Ser263=
NM_181524.2:c.699T>G	NP_852665.1:p.Ser233=