Canonical Allele Identifier: CA359883041

Gene: PIK3R1

Linked Data

• MyVariant Identifiers: chr5:g.67591100A>C (hg19) ; chr5:g.68295272A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295272A>C , CM000667.2:g.68295272A>C	GRCh38
NC_000005.9:g.67591100A>C , CM000667.1:g.67591100A>C	GRCh37
NC_000005.8:g.67626856A>C	NCBI36
NG_012849.2:g.84517A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000320694.13:c.793A>C	ENSP00000323512.8:p.Ser265Arg
ENST00000336483.10:c.883A>C	ENSP00000338554.5:p.Ser295Arg
ENST00000517643.2:c.1693A>C	ENSP00000513333.1:p.Ser565Arg
ENST00000517698.6:c.*663A>C	ENSP00000430424.1:n.*663A>C
ENST00000521657.6:c.1693A>C	ENSP00000429277.1:p.Ser565Arg
ENST00000522084.6:c.883A>C	ENSP00000429766.2:p.Ser295Arg
ENST00000697457.1:c.1618A>C	ENSP00000513315.1:p.Ser540Arg
ENST00000697458.1:c.1693A>C	ENSP00000513316.1:p.Ser565Arg
ENST00000697460.1:c.1168A>C	ENSP00000513318.1:p.Ser390Arg
ENST00000697461.1:c.1693A>C	ENSP00000513319.1:p.Ser565Arg
ENST00000697462.1:c.883A>C	ENSP00000513320.1:p.Ser295Arg
ENST00000697463.1:n.1334A>C
ENST00000697464.1:c.*659A>C	ENSP00000513322.1:n.*659A>C
ENST00000697465.1:c.730A>C	ENSP00000513323.1:p.Ser244Arg
ENST00000697466.1:c.700A>C	ENSP00000513324.1:p.Ser234Arg
ENST00000697467.1:c.604A>C	ENSP00000513325.1:p.Ser202Arg
ENST00000697468.1:c.676A>C	ENSP00000513326.1:p.Ser226Arg
ENST00000697469.1:c.385A>C	ENSP00000513327.1:p.Ser129Arg
ENST00000697470.1:c.289A>C	ENSP00000513328.1:p.Ser97Arg
ENST00000697557.1:c.676A>C	ENSP00000513335.1:p.Ser226Arg
ENST00000521381.6:c.1693A>C MANE Select	ENSP00000428056.1:p.Ser565Arg
ENST00000320694.12:c.793A>C	ENSP00000323512.8:p.Ser265Arg
ENST00000336483.9:c.883A>C	ENSP00000338554.5:p.Ser295Arg
ENST00000517698.5:c.*663A>C	ENSP00000430424.1:n.*663A>C
ENST00000518813.5:n.2236A>C
ENST00000520550.1:n.1092A>C
ENST00000521381.5:c.1693A>C	ENSP00000428056.1:p.Ser565Arg
ENST00000521657.5:c.1693A>C	ENSP00000429277.1:p.Ser565Arg
ENST00000523872.1:c.604A>C	ENSP00000430098.1:p.Ser202Arg
NM_001242466.1:c.604A>C	NP_001229395.1:p.Ser202Arg
NM_181504.3:c.883A>C	NP_852556.2:p.Ser295Arg
NM_181523.2:c.1693A>C	NP_852664.1:p.Ser565Arg
NM_181524.1:c.793A>C	NP_852665.1:p.Ser265Arg
XM_005248542.2:c.1693A>C	XP_005248599.1:p.Ser565Arg
XM_011543493.1:c.1366A>C	XP_011541795.1:p.Ser456Arg
XM_005248542.3:c.1693A>C	XP_005248599.1:p.Ser565Arg
XM_011543493.3:c.1366A>C	XP_011541795.1:p.Ser456Arg
XM_017009585.2:c.1693A>C	XP_016865074.1:p.Ser565Arg
XM_017009586.1:c.1420A>C	XP_016865075.1:p.Ser474Arg
NM_181523.3:c.1693A>C MANE Select	NP_852664.1:p.Ser565Arg
NM_001242466.2:c.604A>C	NP_001229395.1:p.Ser202Arg
NM_181504.4:c.883A>C	NP_852556.2:p.Ser295Arg
NM_181524.2:c.793A>C	NP_852665.1:p.Ser265Arg