Canonical Allele Identifier: CA813423695

Gene: PIK3R1

Linked Data

• dbSNP Id: rs1266912872
• MyVariant Identifiers: chr5:g.67548560G>A (hg19) ; chr5:g.68252732G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68252732G>A , CM000667.2:g.68252732G>A	GRCh38
NC_000005.9:g.67548560G>A , CM000667.1:g.67548560G>A	GRCh37
NC_000005.8:g.67584316G>A	NCBI36
NG_012849.2:g.41977G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517412.2:n.935-20658G>A
ENST00000517643.2:c.335-20658G>A	ENSP00000513333.1:n.335-20658G>A
ENST00000521657.6:c.335-20658G>A	ENSP00000429277.1:n.335-20658G>A
ENST00000697457.1:c.335-20658G>A	ENSP00000513315.1:n.335-20658G>A
ENST00000697458.1:c.335-20658G>A	ENSP00000513316.1:n.335-20658G>A
ENST00000697460.1:c.-191-20658G>A	ENSP00000513318.1:n.-191-20658G>A
ENST00000697461.1:c.335-20658G>A	ENSP00000513319.1:n.335-20658G>A
ENST00000697556.1:c.335-21207G>A	ENSP00000513334.1:n.335-21207G>A
ENST00000521381.6:c.335-20658G>A MANE Select	ENSP00000428056.1:n.335-20658G>A
ENST00000517412.1:n.574-20658G>A
ENST00000520675.1:c.40+12795G>A	ENSP00000428566.1:n.40+12795G>A
ENST00000521381.5:c.335-20658G>A	ENSP00000428056.1:n.335-20658G>A
ENST00000521657.5:c.335-20658G>A	ENSP00000429277.1:n.335-20658G>A
NM_181523.2:c.335-20658G>A	NP_852664.1:n.335-20658G>A
XM_005248542.2:c.335-20658G>A	XP_005248599.1:n.335-20658G>A
XM_011543493.1:c.7+474G>A	XP_011541795.1:n.7+474G>A
XM_005248542.3:c.335-20658G>A	XP_005248599.1:n.335-20658G>A
XM_011543493.3:c.7+474G>A	XP_011541795.1:n.7+474G>A
XM_017009585.2:c.335-20658G>A	XP_016865074.1:n.335-20658G>A
XM_017009586.1:c.61+12795G>A	XP_016865075.1:n.61+12795G>A
NM_181523.3:c.335-20658G>A MANE Select	NP_852664.1:n.335-20658G>A