Canonical Allele Identifier: CA813423641

Gene: PIK3R1

Linked Data

• dbSNP Id: rs1369726725
• MyVariant Identifiers: chr5:g.67548231_67548236del (hg19) ; chr5:g.68252403_68252408del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68252403_68252408del , CM000667.2:g.68252403_68252408del	GRCh38
NC_000005.9:g.67548231_67548236del , CM000667.1:g.67548231_67548236del	GRCh37
NC_000005.8:g.67583987_67583992del	NCBI36
NG_012849.2:g.41648_41653del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517412.2:n.935-20987_935-20982del
ENST00000517643.2:c.335-20987_335-20982del	ENSP00000513333.1:n.335-20987_335-20982del
ENST00000521657.6:c.335-20987_335-20982del	ENSP00000429277.1:n.335-20987_335-20982del
ENST00000697457.1:c.335-20987_335-20982del	ENSP00000513315.1:n.335-20987_335-20982del
ENST00000697458.1:c.335-20987_335-20982del	ENSP00000513316.1:n.335-20987_335-20982del
ENST00000697460.1:c.-191-20987_-191-20982del	ENSP00000513318.1:n.-191-20987_-191-20982del
ENST00000697461.1:c.335-20987_335-20982del	ENSP00000513319.1:n.335-20987_335-20982del
ENST00000697556.1:c.335-21536_335-21531del	ENSP00000513334.1:n.335-21536_335-21531del
ENST00000521381.6:c.335-20987_335-20982del MANE Select	ENSP00000428056.1:n.335-20987_335-20982del
ENST00000517412.1:n.574-20987_574-20982del
ENST00000520675.1:c.40+12466_40+12471del	ENSP00000428566.1:n.40+12466_40+12471del
ENST00000521381.5:c.335-20987_335-20982del	ENSP00000428056.1:n.335-20987_335-20982del
ENST00000521657.5:c.335-20987_335-20982del	ENSP00000429277.1:n.335-20987_335-20982del
NM_181523.2:c.335-20987_335-20982del	NP_852664.1:n.335-20987_335-20982del
XM_005248542.2:c.335-20987_335-20982del	XP_005248599.1:n.335-20987_335-20982del
XM_011543493.1:c.7+145_7+150del	XP_011541795.1:n.7+145_7+150del
XM_005248542.3:c.335-20987_335-20982del	XP_005248599.1:n.335-20987_335-20982del
XM_011543493.3:c.7+145_7+150del	XP_011541795.1:n.7+145_7+150del
XM_017009585.2:c.335-20987_335-20982del	XP_016865074.1:n.335-20987_335-20982del
XM_017009586.1:c.61+12466_61+12471del	XP_016865075.1:n.61+12466_61+12471del
NM_181523.3:c.335-20987_335-20982del MANE Select	NP_852664.1:n.335-20987_335-20982del