Canonical Allele Identifier: CA2576720929
Gene: PIK3R2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156298_18156299del , CM000681.2:g.18156298_18156299del GRCh38
NC_000019.9:g.18267108_18267109del , CM000681.1:g.18267108_18267109del GRCh37
NC_000019.8:g.18128108_18128109del NCBI36
NG_033010.1:g.8121_8122del
NG_033010.2:g.8121_8122del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.322+97_322+98del MANE Select ENSP00000222254.6:n.322+97_322+98del
ENST00000617130.5:c.322+97_322+98del ENSP00000477864.2:n.322+97_322+98del
ENST00000617642.2:c.322+97_322+98del ENSP00000484714.2:n.322+97_322+98del
ENST00000222254.12:c.322+97_322+98del ENSP00000222254.6:n.322+97_322+98del
ENST00000426902.5:c.322+97_322+98del ENSP00000395636.1:n.322+97_322+98del
ENST00000593731.1:c.322+97_322+98del ENSP00000471914.1:n.322+97_322+98del
ENST00000617130.4:c.322+97_322+98del ENSP00000477864.1:n.322+97_322+98del
ENST00000617642.1:c.322+97_322+98del ENSP00000484714.1:n.322+97_322+98del
NM_005027.3:c.322+97_322+98del NP_005018.1:n.322+97_322+98del
NR_073517.1:n.862+97_862+98del
NM_005027.4:c.322+97_322+98del MANE Select NP_005018.2:n.322+97_322+98del
NR_073517.2:n.877+97_877+98del
NR_162071.1:n.877+97_877+98del