Canonical Allele Identifier: CA1077129958

Gene: PIK3R1

Linked Data

• gnomAD v3: 5-68252364-T-TA
• gnomAD v4: 5-68252364-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68252364_68252365insA , CM000667.2:g.68252364_68252365insA	GRCh38
NC_000005.9:g.67548192_67548193insA , CM000667.1:g.67548192_67548193insA	GRCh37
NC_000005.8:g.67583948_67583949insA	NCBI36
NG_012849.2:g.41609_41610insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517412.2:n.935-21026_935-21025insA
ENST00000517643.2:c.335-21026_335-21025insA	ENSP00000513333.1:n.335-21026_335-21025insA
ENST00000521657.6:c.335-21026_335-21025insA	ENSP00000429277.1:n.335-21026_335-21025insA
ENST00000697457.1:c.335-21026_335-21025insA	ENSP00000513315.1:n.335-21026_335-21025insA
ENST00000697458.1:c.335-21026_335-21025insA	ENSP00000513316.1:n.335-21026_335-21025insA
ENST00000697460.1:c.-191-21026_-191-21025insA	ENSP00000513318.1:n.-191-21026_-191-21025insA
ENST00000697461.1:c.335-21026_335-21025insA	ENSP00000513319.1:n.335-21026_335-21025insA
ENST00000697556.1:c.335-21575_335-21574insA	ENSP00000513334.1:n.335-21575_335-21574insA
ENST00000521381.6:c.335-21026_335-21025insA MANE Select	ENSP00000428056.1:n.335-21026_335-21025insA
ENST00000517412.1:n.574-21026_574-21025insA
ENST00000520675.1:c.40+12427_40+12428insA	ENSP00000428566.1:n.40+12427_40+12428insA
ENST00000521381.5:c.335-21026_335-21025insA	ENSP00000428056.1:n.335-21026_335-21025insA
ENST00000521657.5:c.335-21026_335-21025insA	ENSP00000429277.1:n.335-21026_335-21025insA
NM_181523.2:c.335-21026_335-21025insA	NP_852664.1:n.335-21026_335-21025insA
XM_005248542.2:c.335-21026_335-21025insA	XP_005248599.1:n.335-21026_335-21025insA
XM_011543493.1:c.7+106_7+107insA	XP_011541795.1:n.7+106_7+107insA
XM_005248542.3:c.335-21026_335-21025insA	XP_005248599.1:n.335-21026_335-21025insA
XM_011543493.3:c.7+106_7+107insA	XP_011541795.1:n.7+106_7+107insA
XM_017009585.2:c.335-21026_335-21025insA	XP_016865074.1:n.335-21026_335-21025insA
XM_017009586.1:c.61+12427_61+12428insA	XP_016865075.1:n.61+12427_61+12428insA
NM_181523.3:c.335-21026_335-21025insA MANE Select	NP_852664.1:n.335-21026_335-21025insA