Canonical Allele Identifier: CA1553387737
Gene: PIK3R1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.68252386_68252389delinsTGGG , CM000667.2:g.68252386_68252389delinsTGGG GRCh38
NC_000005.9:g.67548214_67548217delinsTGGG , CM000667.1:g.67548214_67548217delinsTGGG GRCh37
NC_000005.8:g.67583970_67583973delinsTGGG NCBI36
NG_012849.2:g.41631_41634delinsTGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000517412.2:n.935-21004_935-21001delinsTGGG
ENST00000517643.2:c.335-21004_335-21001delinsTGGG ENSP00000513333.1:n.335-21004_335-21001delinsTGGG
ENST00000521657.6:c.335-21004_335-21001delinsTGGG ENSP00000429277.1:n.335-21004_335-21001delinsTGGG
ENST00000697457.1:c.335-21004_335-21001delinsTGGG ENSP00000513315.1:n.335-21004_335-21001delinsTGGG
ENST00000697458.1:c.335-21004_335-21001delinsTGGG ENSP00000513316.1:n.335-21004_335-21001delinsTGGG
ENST00000697460.1:c.-191-21004_-191-21001delinsTGGG ENSP00000513318.1:n.-191-21004_-191-21001delinsTGGG
ENST00000697461.1:c.335-21004_335-21001delinsTGGG ENSP00000513319.1:n.335-21004_335-21001delinsTGGG
ENST00000697556.1:c.335-21553_335-21550delinsTGGG ENSP00000513334.1:n.335-21553_335-21550delinsTGGG
ENST00000521381.6:c.335-21004_335-21001delinsTGGG MANE Select ENSP00000428056.1:n.335-21004_335-21001delinsTGGG
ENST00000517412.1:n.574-21004_574-21001delinsTGGG
ENST00000520675.1:c.40+12449_40+12452delinsTGGG ENSP00000428566.1:n.40+12449_40+12452delinsTGGG
ENST00000521381.5:c.335-21004_335-21001delinsTGGG ENSP00000428056.1:n.335-21004_335-21001delinsTGGG
ENST00000521657.5:c.335-21004_335-21001delinsTGGG ENSP00000429277.1:n.335-21004_335-21001delinsTGGG
NM_181523.2:c.335-21004_335-21001delinsTGGG NP_852664.1:n.335-21004_335-21001delinsTGGG
XM_005248542.2:c.335-21004_335-21001delinsTGGG XP_005248599.1:n.335-21004_335-21001delinsTGGG
XM_011543493.1:c.7+128_7+131delinsTGGG XP_011541795.1:n.7+128_7+131delinsTGGG
XM_005248542.3:c.335-21004_335-21001delinsTGGG XP_005248599.1:n.335-21004_335-21001delinsTGGG
XM_011543493.3:c.7+128_7+131delinsTGGG XP_011541795.1:n.7+128_7+131delinsTGGG
XM_017009585.2:c.335-21004_335-21001delinsTGGG XP_016865074.1:n.335-21004_335-21001delinsTGGG
XM_017009586.1:c.61+12449_61+12452delinsTGGG XP_016865075.1:n.61+12449_61+12452delinsTGGG
NM_181523.3:c.335-21004_335-21001delinsTGGG MANE Select NP_852664.1:n.335-21004_335-21001delinsTGGG