Canonical Allele Identifier: CA1553386109
Gene: PIK3R1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.68250576_68250581delinsCAATGT , CM000667.2:g.68250576_68250581delinsCAATGT GRCh38
NC_000005.9:g.67546404_67546409delinsCAATGT , CM000667.1:g.67546404_67546409delinsCAATGT GRCh37
NC_000005.8:g.67582160_67582165delinsCAATGT NCBI36
NG_012849.2:g.39821_39826delinsCAATGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000517412.2:n.935-22814_935-22809delinsCAATGT
ENST00000517643.2:c.335-22814_335-22809delinsCAATGT ENSP00000513333.1:n.335-22814_335-22809delinsCAATGT
ENST00000521657.6:c.335-22814_335-22809delinsCAATGT ENSP00000429277.1:n.335-22814_335-22809delinsCAATGT
ENST00000697457.1:c.335-22814_335-22809delinsCAATGT ENSP00000513315.1:n.335-22814_335-22809delinsCAATGT
ENST00000697458.1:c.335-22814_335-22809delinsCAATGT ENSP00000513316.1:n.335-22814_335-22809delinsCAATGT
ENST00000697460.1:c.-192+22377_-192+22382delinsCAATGT ENSP00000513318.1:n.-192+22377_-192+22382delinsCAATGT
ENST00000697461.1:c.335-22814_335-22809delinsCAATGT ENSP00000513319.1:n.335-22814_335-22809delinsCAATGT
ENST00000697556.1:c.335-23363_335-23358delinsCAATGT ENSP00000513334.1:n.335-23363_335-23358delinsCAATGT
ENST00000521381.6:c.335-22814_335-22809delinsCAATGT MANE Select ENSP00000428056.1:n.335-22814_335-22809delinsCAATGT
ENST00000517412.1:n.574-22814_574-22809delinsCAATGT
ENST00000520675.1:c.40+10639_40+10644delinsCAATGT ENSP00000428566.1:n.40+10639_40+10644delinsCAATGT
ENST00000521381.5:c.335-22814_335-22809delinsCAATGT ENSP00000428056.1:n.335-22814_335-22809delinsCAATGT
ENST00000521657.5:c.335-22814_335-22809delinsCAATGT ENSP00000429277.1:n.335-22814_335-22809delinsCAATGT
NM_181523.2:c.335-22814_335-22809delinsCAATGT NP_852664.1:n.335-22814_335-22809delinsCAATGT
XM_005248542.2:c.335-22814_335-22809delinsCAATGT XP_005248599.1:n.335-22814_335-22809delinsCAATGT
XM_005248542.3:c.335-22814_335-22809delinsCAATGT XP_005248599.1:n.335-22814_335-22809delinsCAATGT
XM_017009585.2:c.335-22814_335-22809delinsCAATGT XP_016865074.1:n.335-22814_335-22809delinsCAATGT
XM_017009586.1:c.61+10639_61+10644delinsCAATGT XP_016865075.1:n.61+10639_61+10644delinsCAATGT
NM_181523.3:c.335-22814_335-22809delinsCAATGT MANE Select NP_852664.1:n.335-22814_335-22809delinsCAATGT