Canonical Allele Identifier: CA560224429

Gene: PIK3R1

Linked Data

• dbSNP Id: rs1201390326
• gnomAD v2: 5-67548197-T-TA
• gnomAD v3: 5-68252369-T-TA
• gnomAD v4: 5-68252369-T-TA
• MyVariant Identifiers: chr5:g.67548197_67548198insA (hg19) ; chr5:g.68252369_68252370insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.68252369_68252370insA , CM000667.2:g.68252369_68252370insA	GRCh38
NC_000005.9:g.67548197_67548198insA , CM000667.1:g.67548197_67548198insA	GRCh37
NC_000005.8:g.67583953_67583954insA	NCBI36
NG_012849.2:g.41614_41615insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517412.2:n.935-21021_935-21020insA
ENST00000517643.2:c.335-21021_335-21020insA	ENSP00000513333.1:n.335-21021_335-21020insA
ENST00000521657.6:c.335-21021_335-21020insA	ENSP00000429277.1:n.335-21021_335-21020insA
ENST00000697457.1:c.335-21021_335-21020insA	ENSP00000513315.1:n.335-21021_335-21020insA
ENST00000697458.1:c.335-21021_335-21020insA	ENSP00000513316.1:n.335-21021_335-21020insA
ENST00000697460.1:c.-191-21021_-191-21020insA	ENSP00000513318.1:n.-191-21021_-191-21020insA
ENST00000697461.1:c.335-21021_335-21020insA	ENSP00000513319.1:n.335-21021_335-21020insA
ENST00000697556.1:c.335-21570_335-21569insA	ENSP00000513334.1:n.335-21570_335-21569insA
ENST00000521381.6:c.335-21021_335-21020insA MANE Select	ENSP00000428056.1:n.335-21021_335-21020insA
ENST00000517412.1:n.574-21021_574-21020insA
ENST00000520675.1:c.40+12432_40+12433insA	ENSP00000428566.1:n.40+12432_40+12433insA
ENST00000521381.5:c.335-21021_335-21020insA	ENSP00000428056.1:n.335-21021_335-21020insA
ENST00000521657.5:c.335-21021_335-21020insA	ENSP00000429277.1:n.335-21021_335-21020insA
NM_181523.2:c.335-21021_335-21020insA	NP_852664.1:n.335-21021_335-21020insA
XM_005248542.2:c.335-21021_335-21020insA	XP_005248599.1:n.335-21021_335-21020insA
XM_011543493.1:c.7+111_7+112insA	XP_011541795.1:n.7+111_7+112insA
XM_005248542.3:c.335-21021_335-21020insA	XP_005248599.1:n.335-21021_335-21020insA
XM_011543493.3:c.7+111_7+112insA	XP_011541795.1:n.7+111_7+112insA
XM_017009585.2:c.335-21021_335-21020insA	XP_016865074.1:n.335-21021_335-21020insA
XM_017009586.1:c.61+12432_61+12433insA	XP_016865075.1:n.61+12432_61+12433insA
NM_181523.3:c.335-21021_335-21020insA MANE Select	NP_852664.1:n.335-21021_335-21020insA