Canonical Allele Identifier: CA1553397379
Gene: PIK3R1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.68280983G= , CM000667.2:g.68280983G= GRCh38
NC_000005.9:g.67576811G= , CM000667.1:g.67576811G= GRCh37
NC_000005.8:g.67612567G= NCBI36
NG_012849.2:g.70228G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000517643.2:c.893G= ENSP00000513333.1:p.Trp298=
ENST00000521657.6:c.893G= ENSP00000429277.1:p.Trp298=
ENST00000522084.6:c.83G= ENSP00000429766.2:p.Trp28=
ENST00000697457.1:c.818G= ENSP00000513315.1:p.Trp273=
ENST00000697458.1:c.893G= ENSP00000513316.1:p.Trp298=
ENST00000697460.1:c.368G= ENSP00000513318.1:p.Trp123=
ENST00000697461.1:c.893G= ENSP00000513319.1:p.Trp298=
ENST00000697556.1:c.800G= ENSP00000513334.1:p.Trp267=
ENST00000521381.6:c.893G= MANE Select ENSP00000428056.1:p.Trp298=
ENST00000521381.5:c.893G= ENSP00000428056.1:p.Trp298=
ENST00000521657.5:c.893G= ENSP00000429277.1:p.Trp298=
ENST00000522084.5:c.83G= ENSP00000429766.1:p.Trp28=
ENST00000523807.5:c.83G= ENSP00000430126.1:p.Trp28=
NM_181523.2:c.893G= NP_852664.1:p.Trp298=
XM_005248542.2:c.893G= XP_005248599.1:p.Trp298=
XM_011543493.1:c.566G= XP_011541795.1:p.Trp189=
XM_005248542.3:c.893G= XP_005248599.1:p.Trp298=
XM_011543493.3:c.566G= XP_011541795.1:p.Trp189=
XM_017009585.2:c.893G= XP_016865074.1:p.Trp298=
XM_017009586.1:c.620G= XP_016865075.1:p.Trp207=
NM_181523.3:c.893G= MANE Select NP_852664.1:p.Trp298=