Canonical Allele Identifier: CA1553387703
Gene: PIK3R1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.68252372_68252373delinsCA , CM000667.2:g.68252372_68252373delinsCA GRCh38
NC_000005.9:g.67548200_67548201delinsCA , CM000667.1:g.67548200_67548201delinsCA GRCh37
NC_000005.8:g.67583956_67583957delinsCA NCBI36
NG_012849.2:g.41617_41618delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000517412.2:n.935-21018_935-21017delinsCA
ENST00000517643.2:c.335-21018_335-21017delinsCA ENSP00000513333.1:n.335-21018_335-21017delinsCA
ENST00000521657.6:c.335-21018_335-21017delinsCA ENSP00000429277.1:n.335-21018_335-21017delinsCA
ENST00000697457.1:c.335-21018_335-21017delinsCA ENSP00000513315.1:n.335-21018_335-21017delinsCA
ENST00000697458.1:c.335-21018_335-21017delinsCA ENSP00000513316.1:n.335-21018_335-21017delinsCA
ENST00000697460.1:c.-191-21018_-191-21017delinsCA ENSP00000513318.1:n.-191-21018_-191-21017delinsCA
ENST00000697461.1:c.335-21018_335-21017delinsCA ENSP00000513319.1:n.335-21018_335-21017delinsCA
ENST00000697556.1:c.335-21567_335-21566delinsCA ENSP00000513334.1:n.335-21567_335-21566delinsCA
ENST00000521381.6:c.335-21018_335-21017delinsCA MANE Select ENSP00000428056.1:n.335-21018_335-21017delinsCA
ENST00000517412.1:n.574-21018_574-21017delinsCA
ENST00000520675.1:c.40+12435_40+12436delinsCA ENSP00000428566.1:n.40+12435_40+12436delinsCA
ENST00000521381.5:c.335-21018_335-21017delinsCA ENSP00000428056.1:n.335-21018_335-21017delinsCA
ENST00000521657.5:c.335-21018_335-21017delinsCA ENSP00000429277.1:n.335-21018_335-21017delinsCA
NM_181523.2:c.335-21018_335-21017delinsCA NP_852664.1:n.335-21018_335-21017delinsCA
XM_005248542.2:c.335-21018_335-21017delinsCA XP_005248599.1:n.335-21018_335-21017delinsCA
XM_011543493.1:c.7+114_7+115delinsCA XP_011541795.1:n.7+114_7+115delinsCA
XM_005248542.3:c.335-21018_335-21017delinsCA XP_005248599.1:n.335-21018_335-21017delinsCA
XM_011543493.3:c.7+114_7+115delinsCA XP_011541795.1:n.7+114_7+115delinsCA
XM_017009585.2:c.335-21018_335-21017delinsCA XP_016865074.1:n.335-21018_335-21017delinsCA
XM_017009586.1:c.61+12435_61+12436delinsCA XP_016865075.1:n.61+12435_61+12436delinsCA
NM_181523.3:c.335-21018_335-21017delinsCA MANE Select NP_852664.1:n.335-21018_335-21017delinsCA