Canonical Allele Identifier: CA1553387834

Gene: PIK3R1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68252480_68252483delinsTGTG , CM000667.2:g.68252480_68252483delinsTGTG	GRCh38
NC_000005.9:g.67548308_67548311delinsTGTG , CM000667.1:g.67548308_67548311delinsTGTG	GRCh37
NC_000005.8:g.67584064_67584067delinsTGTG	NCBI36
NG_012849.2:g.41725_41728delinsTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517412.2:n.935-20910_935-20907delinsTGTG
ENST00000517643.2:c.335-20910_335-20907delinsTGTG	ENSP00000513333.1:n.335-20910_335-20907delinsTGTG
ENST00000521657.6:c.335-20910_335-20907delinsTGTG	ENSP00000429277.1:n.335-20910_335-20907delinsTGTG
ENST00000697457.1:c.335-20910_335-20907delinsTGTG	ENSP00000513315.1:n.335-20910_335-20907delinsTGTG
ENST00000697458.1:c.335-20910_335-20907delinsTGTG	ENSP00000513316.1:n.335-20910_335-20907delinsTGTG
ENST00000697460.1:c.-191-20910_-191-20907delinsTGTG	ENSP00000513318.1:n.-191-20910_-191-20907delinsTGTG
ENST00000697461.1:c.335-20910_335-20907delinsTGTG	ENSP00000513319.1:n.335-20910_335-20907delinsTGTG
ENST00000697556.1:c.335-21459_335-21456delinsTGTG	ENSP00000513334.1:n.335-21459_335-21456delinsTGTG
ENST00000521381.6:c.335-20910_335-20907delinsTGTG MANE Select	ENSP00000428056.1:n.335-20910_335-20907delinsTGTG
ENST00000517412.1:n.574-20910_574-20907delinsTGTG
ENST00000520675.1:c.40+12543_40+12546delinsTGTG	ENSP00000428566.1:n.40+12543_40+12546delinsTGTG
ENST00000521381.5:c.335-20910_335-20907delinsTGTG	ENSP00000428056.1:n.335-20910_335-20907delinsTGTG
ENST00000521657.5:c.335-20910_335-20907delinsTGTG	ENSP00000429277.1:n.335-20910_335-20907delinsTGTG
NM_181523.2:c.335-20910_335-20907delinsTGTG	NP_852664.1:n.335-20910_335-20907delinsTGTG
XM_005248542.2:c.335-20910_335-20907delinsTGTG	XP_005248599.1:n.335-20910_335-20907delinsTGTG
XM_011543493.1:c.7+222_7+225delinsTGTG	XP_011541795.1:n.7+222_7+225delinsTGTG
XM_005248542.3:c.335-20910_335-20907delinsTGTG	XP_005248599.1:n.335-20910_335-20907delinsTGTG
XM_011543493.3:c.7+222_7+225delinsTGTG	XP_011541795.1:n.7+222_7+225delinsTGTG
XM_017009585.2:c.335-20910_335-20907delinsTGTG	XP_016865074.1:n.335-20910_335-20907delinsTGTG
XM_017009586.1:c.61+12543_61+12546delinsTGTG	XP_016865075.1:n.61+12543_61+12546delinsTGTG
NM_181523.3:c.335-20910_335-20907delinsTGTG MANE Select	NP_852664.1:n.335-20910_335-20907delinsTGTG