Canonical Allele Identifier: CA813423112

Gene: PIK3R1

Linked Data

• dbSNP Id: rs1280891169
• MyVariant Identifiers: chr5:g.67546451T>G (hg19) ; chr5:g.68250623T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68250623T>G , CM000667.2:g.68250623T>G	GRCh38
NC_000005.9:g.67546451T>G , CM000667.1:g.67546451T>G	GRCh37
NC_000005.8:g.67582207T>G	NCBI36
NG_012849.2:g.39868T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000517412.2:n.935-22767T>G
ENST00000517643.2:c.335-22767T>G	ENSP00000513333.1:n.335-22767T>G
ENST00000521657.6:c.335-22767T>G	ENSP00000429277.1:n.335-22767T>G
ENST00000697457.1:c.335-22767T>G	ENSP00000513315.1:n.335-22767T>G
ENST00000697458.1:c.335-22767T>G	ENSP00000513316.1:n.335-22767T>G
ENST00000697460.1:c.-192+22424T>G	ENSP00000513318.1:n.-192+22424T>G
ENST00000697461.1:c.335-22767T>G	ENSP00000513319.1:n.335-22767T>G
ENST00000697556.1:c.335-23316T>G	ENSP00000513334.1:n.335-23316T>G
ENST00000521381.6:c.335-22767T>G MANE Select	ENSP00000428056.1:n.335-22767T>G
ENST00000517412.1:n.574-22767T>G
ENST00000520675.1:c.40+10686T>G	ENSP00000428566.1:n.40+10686T>G
ENST00000521381.5:c.335-22767T>G	ENSP00000428056.1:n.335-22767T>G
ENST00000521657.5:c.335-22767T>G	ENSP00000429277.1:n.335-22767T>G
NM_181523.2:c.335-22767T>G	NP_852664.1:n.335-22767T>G
XM_005248542.2:c.335-22767T>G	XP_005248599.1:n.335-22767T>G
XM_005248542.3:c.335-22767T>G	XP_005248599.1:n.335-22767T>G
XM_017009585.2:c.335-22767T>G	XP_016865074.1:n.335-22767T>G
XM_017009586.1:c.61+10686T>G	XP_016865075.1:n.61+10686T>G
NM_181523.3:c.335-22767T>G MANE Select	NP_852664.1:n.335-22767T>G