Canonical Allele Identifier: CA9306965

Gene: PIK3R2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18163151C>T , CM000681.2:g.18163151C>T	GRCh38
NC_000019.9:g.18273961C>T , CM000681.1:g.18273961C>T	GRCh37
NC_000019.8:g.18134961C>T	NCBI36
NG_033010.1:g.14974C>T
NG_033010.2:g.14974C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005027.4:c.1290+4C>T MANE Select	NP_005018.2:n.1290+4C>T
ENST00000222254.13:c.1290+4C>T MANE Select	ENSP00000222254.6:n.1290+4C>T
NM_005027.3:c.1290+4C>T	NP_005018.1:n.1290+4C>T
NR_073517.1:n.1830+4C>T
NR_073517.2:n.1845+4C>T
NR_162071.1:n.1628+4C>T
ENST00000222254.12:c.1290+4C>T	ENSP00000222254.6:n.1290+4C>T
ENST00000426902.5:c.1290+4C>T	ENSP00000395636.1:n.1290+4C>T
ENST00000593731.1:c.1290+4C>T	ENSP00000471914.1:n.1290+4C>T
ENST00000617130.4:c.1290+4C>T	ENSP00000477864.1:n.1290+4C>T
ENST00000617130.5:c.*269+4C>T	ENSP00000477864.2:n.*269+4C>T
ENST00000617642.1:c.1290+4C>T	ENSP00000484714.1:n.1290+4C>T
ENST00000617642.2:c.*269+4C>T	ENSP00000484714.2:n.*269+4C>T
ENST00000672815.1:c.3+4C>T	ENSP00000500792.1:n.3+4C>T
ENST00000675271.1:n.240C>T