Canonical Allele Identifier: CA359883046

Gene: PIK3R1

Linked Data

• COSMIC: COSM5514170 ; COSM5514171 ; COSM5514172
• MyVariant Identifiers: chr5:g.67591101G>T (hg19) ; chr5:g.68295273G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68295273G>T , CM000667.2:g.68295273G>T	GRCh38
NC_000005.9:g.67591101G>T , CM000667.1:g.67591101G>T	GRCh37
NC_000005.8:g.67626857G>T	NCBI36
NG_012849.2:g.84518G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320694.13:c.794G>T	ENSP00000323512.8:p.Ser265Ile
ENST00000336483.10:c.884G>T	ENSP00000338554.5:p.Ser295Ile
ENST00000517643.2:c.1694G>T	ENSP00000513333.1:p.Ser565Ile
ENST00000517698.6:c.*664G>T	ENSP00000430424.1:n.*664G>T
ENST00000521657.6:c.1694G>T	ENSP00000429277.1:p.Ser565Ile
ENST00000522084.6:c.884G>T	ENSP00000429766.2:p.Ser295Ile
ENST00000697457.1:c.1619G>T	ENSP00000513315.1:p.Ser540Ile
ENST00000697458.1:c.1694G>T	ENSP00000513316.1:p.Ser565Ile
ENST00000697460.1:c.1169G>T	ENSP00000513318.1:p.Ser390Ile
ENST00000697461.1:c.1694G>T	ENSP00000513319.1:p.Ser565Ile
ENST00000697462.1:c.884G>T	ENSP00000513320.1:p.Ser295Ile
ENST00000697463.1:n.1335G>T
ENST00000697464.1:c.*660G>T	ENSP00000513322.1:n.*660G>T
ENST00000697465.1:c.731G>T	ENSP00000513323.1:p.Ser244Ile
ENST00000697466.1:c.701G>T	ENSP00000513324.1:p.Ser234Ile
ENST00000697467.1:c.605G>T	ENSP00000513325.1:p.Ser202Ile
ENST00000697468.1:c.677G>T	ENSP00000513326.1:p.Ser226Ile
ENST00000697469.1:c.386G>T	ENSP00000513327.1:p.Ser129Ile
ENST00000697470.1:c.290G>T	ENSP00000513328.1:p.Ser97Ile
ENST00000697557.1:c.677G>T	ENSP00000513335.1:p.Ser226Ile
ENST00000521381.6:c.1694G>T MANE Select	ENSP00000428056.1:p.Ser565Ile
ENST00000320694.12:c.794G>T	ENSP00000323512.8:p.Ser265Ile
ENST00000336483.9:c.884G>T	ENSP00000338554.5:p.Ser295Ile
ENST00000517698.5:c.*664G>T	ENSP00000430424.1:n.*664G>T
ENST00000518813.5:n.2237G>T
ENST00000520550.1:n.1093G>T
ENST00000521381.5:c.1694G>T	ENSP00000428056.1:p.Ser565Ile
ENST00000521657.5:c.1694G>T	ENSP00000429277.1:p.Ser565Ile
ENST00000523872.1:c.605G>T	ENSP00000430098.1:p.Ser202Ile
NM_001242466.1:c.605G>T	NP_001229395.1:p.Ser202Ile
NM_181504.3:c.884G>T	NP_852556.2:p.Ser295Ile
NM_181523.2:c.1694G>T	NP_852664.1:p.Ser565Ile
NM_181524.1:c.794G>T	NP_852665.1:p.Ser265Ile
XM_005248542.2:c.1694G>T	XP_005248599.1:p.Ser565Ile
XM_011543493.1:c.1367G>T	XP_011541795.1:p.Ser456Ile
XM_005248542.3:c.1694G>T	XP_005248599.1:p.Ser565Ile
XM_011543493.3:c.1367G>T	XP_011541795.1:p.Ser456Ile
XM_017009585.2:c.1694G>T	XP_016865074.1:p.Ser565Ile
XM_017009586.1:c.1421G>T	XP_016865075.1:p.Ser474Ile
NM_181523.3:c.1694G>T MANE Select	NP_852664.1:p.Ser565Ile
NM_001242466.2:c.605G>T	NP_001229395.1:p.Ser202Ile
NM_181504.4:c.884G>T	NP_852556.2:p.Ser295Ile
NM_181524.2:c.794G>T	NP_852665.1:p.Ser265Ile