Canonical Allele Identifier: CA359873078
Community Standard Title: NM_181523.3(PIK3R1):c.484C>T (p.Arg162Ter)
Gene: PIK3R1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.68273995C>T , CM000667.2:g.68273995C>T GRCh38
NC_000005.9:g.67569823C>T , CM000667.1:g.67569823C>T GRCh37
NC_000005.8:g.67605579C>T NCBI36
NG_012849.2:g.63240C>T

Transcript Alleles

HGVS Amino-acid Change
NM_181523.3:c.484C>T MANE Select NP_852664.1:p.Arg162Ter
ENST00000521381.6:c.484C>T MANE Select ENSP00000428056.1:p.Arg162Ter
NM_181523.2:c.484C>T NP_852664.1:p.Arg162Ter
ENST00000517412.2:n.1540C>T
ENST00000517643.2:c.484C>T ENSP00000513333.1:p.Arg162Ter
ENST00000520675.1:c.190C>T ENSP00000428566.1:p.Arg64Ter
ENST00000521381.5:c.484C>T ENSP00000428056.1:p.Arg162Ter
ENST00000521657.5:c.484C>T ENSP00000429277.1:p.Arg162Ter
ENST00000521657.6:c.484C>T ENSP00000429277.1:p.Arg162Ter
ENST00000697457.1:c.427+513C>T ENSP00000513315.1:n.427+513C>T
ENST00000697458.1:c.484C>T ENSP00000513316.1:p.Arg162Ter
ENST00000697460.1:c.-42C>T ENSP00000513318.1:n.-42C>T
ENST00000697461.1:c.484C>T ENSP00000513319.1:p.Arg162Ter
ENST00000697556.1:c.391C>T ENSP00000513334.1:p.Arg131Ter
XM_005248542.2:c.484C>T XP_005248599.1:p.Arg162Ter
XM_005248542.3:c.484C>T XP_005248599.1:p.Arg162Ter
XM_011543493.1:c.157C>T XP_011541795.1:p.Arg53Ter
XM_011543493.3:c.157C>T XP_011541795.1:p.Arg53Ter
XM_017009585.2:c.484C>T XP_016865074.1:p.Arg162Ter
XM_017009586.1:c.211C>T XP_016865075.1:p.Arg71Ter