Canonical Allele Identifier: CA1077130001

Gene: PIK3R1

Linked Data

• gnomAD v3: 5-68252370-T-TAA
• gnomAD v4: 5-68252370-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68252371_68252372insAA , CM000667.2:g.68252371_68252372insAA	GRCh38
NC_000005.9:g.67548199_67548200insAA , CM000667.1:g.67548199_67548200insAA	GRCh37
NC_000005.8:g.67583955_67583956insAA	NCBI36
NG_012849.2:g.41616_41617insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517412.2:n.935-21019_935-21018insAA
ENST00000517643.2:c.335-21019_335-21018insAA	ENSP00000513333.1:n.335-21019_335-21018insAA
ENST00000521657.6:c.335-21019_335-21018insAA	ENSP00000429277.1:n.335-21019_335-21018insAA
ENST00000697457.1:c.335-21019_335-21018insAA	ENSP00000513315.1:n.335-21019_335-21018insAA
ENST00000697458.1:c.335-21019_335-21018insAA	ENSP00000513316.1:n.335-21019_335-21018insAA
ENST00000697460.1:c.-191-21019_-191-21018insAA	ENSP00000513318.1:n.-191-21019_-191-21018insAA
ENST00000697461.1:c.335-21019_335-21018insAA	ENSP00000513319.1:n.335-21019_335-21018insAA
ENST00000697556.1:c.335-21568_335-21567insAA	ENSP00000513334.1:n.335-21568_335-21567insAA
ENST00000521381.6:c.335-21019_335-21018insAA MANE Select	ENSP00000428056.1:n.335-21019_335-21018insAA
ENST00000517412.1:n.574-21019_574-21018insAA
ENST00000520675.1:c.40+12434_40+12435insAA	ENSP00000428566.1:n.40+12434_40+12435insAA
ENST00000521381.5:c.335-21019_335-21018insAA	ENSP00000428056.1:n.335-21019_335-21018insAA
ENST00000521657.5:c.335-21019_335-21018insAA	ENSP00000429277.1:n.335-21019_335-21018insAA
NM_181523.2:c.335-21019_335-21018insAA	NP_852664.1:n.335-21019_335-21018insAA
XM_005248542.2:c.335-21019_335-21018insAA	XP_005248599.1:n.335-21019_335-21018insAA
XM_011543493.1:c.7+113_7+114insAA	XP_011541795.1:n.7+113_7+114insAA
XM_005248542.3:c.335-21019_335-21018insAA	XP_005248599.1:n.335-21019_335-21018insAA
XM_011543493.3:c.7+113_7+114insAA	XP_011541795.1:n.7+113_7+114insAA
XM_017009585.2:c.335-21019_335-21018insAA	XP_016865074.1:n.335-21019_335-21018insAA
XM_017009586.1:c.61+12434_61+12435insAA	XP_016865075.1:n.61+12434_61+12435insAA
NM_181523.3:c.335-21019_335-21018insAA MANE Select	NP_852664.1:n.335-21019_335-21018insAA