Canonical Allele Identifier: CA1553387578

Gene: PIK3R1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68252270_68252271delinsCA , CM000667.2:g.68252270_68252271delinsCA	GRCh38
NC_000005.9:g.67548098_67548099delinsCA , CM000667.1:g.67548098_67548099delinsCA	GRCh37
NC_000005.8:g.67583854_67583855delinsCA	NCBI36
NG_012849.2:g.41515_41516delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517412.2:n.935-21120_935-21119delinsCA
ENST00000517643.2:c.335-21120_335-21119delinsCA	ENSP00000513333.1:n.335-21120_335-21119delinsCA
ENST00000521657.6:c.335-21120_335-21119delinsCA	ENSP00000429277.1:n.335-21120_335-21119delinsCA
ENST00000697457.1:c.335-21120_335-21119delinsCA	ENSP00000513315.1:n.335-21120_335-21119delinsCA
ENST00000697458.1:c.335-21120_335-21119delinsCA	ENSP00000513316.1:n.335-21120_335-21119delinsCA
ENST00000697460.1:c.-191-21120_-191-21119delinsCA	ENSP00000513318.1:n.-191-21120_-191-21119delinsCA
ENST00000697461.1:c.335-21120_335-21119delinsCA	ENSP00000513319.1:n.335-21120_335-21119delinsCA
ENST00000697556.1:c.335-21669_335-21668delinsCA	ENSP00000513334.1:n.335-21669_335-21668delinsCA
ENST00000521381.6:c.335-21120_335-21119delinsCA MANE Select	ENSP00000428056.1:n.335-21120_335-21119delinsCA
ENST00000517412.1:n.574-21120_574-21119delinsCA
ENST00000520675.1:c.40+12333_40+12334delinsCA	ENSP00000428566.1:n.40+12333_40+12334delinsCA
ENST00000521381.5:c.335-21120_335-21119delinsCA	ENSP00000428056.1:n.335-21120_335-21119delinsCA
ENST00000521657.5:c.335-21120_335-21119delinsCA	ENSP00000429277.1:n.335-21120_335-21119delinsCA
NM_181523.2:c.335-21120_335-21119delinsCA	NP_852664.1:n.335-21120_335-21119delinsCA
XM_005248542.2:c.335-21120_335-21119delinsCA	XP_005248599.1:n.335-21120_335-21119delinsCA
XM_011543493.1:c.7+12_7+13delinsCA	XP_011541795.1:n.7+12_7+13delinsCA
XM_005248542.3:c.335-21120_335-21119delinsCA	XP_005248599.1:n.335-21120_335-21119delinsCA
XM_011543493.3:c.7+12_7+13delinsCA	XP_011541795.1:n.7+12_7+13delinsCA
XM_017009585.2:c.335-21120_335-21119delinsCA	XP_016865074.1:n.335-21120_335-21119delinsCA
XM_017009586.1:c.61+12333_61+12334delinsCA	XP_016865075.1:n.61+12333_61+12334delinsCA
NM_181523.3:c.335-21120_335-21119delinsCA MANE Select	NP_852664.1:n.335-21120_335-21119delinsCA