Canonical Allele Identifier: CA2583525551
Gene: PIK3R2 HGNC NCBI

Linked Data

gnomAD v4: 19-18156344-C-CCTG
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156344_18156345insCTG , CM000681.2:g.18156344_18156345insCTG GRCh38
NC_000019.9:g.18267154_18267155insCTG , CM000681.1:g.18267154_18267155insCTG GRCh37
NC_000019.8:g.18128154_18128155insCTG NCBI36
NG_033010.1:g.8167_8168insCTG
NG_033010.2:g.8167_8168insCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.322+143_322+144insCTG MANE Select ENSP00000222254.6:n.322+143_322+144insCTG
ENST00000617130.5:c.322+143_322+144insCTG ENSP00000477864.2:n.322+143_322+144insCTG
ENST00000617642.2:c.322+143_322+144insCTG ENSP00000484714.2:n.322+143_322+144insCTG
ENST00000222254.12:c.322+143_322+144insCTG ENSP00000222254.6:n.322+143_322+144insCTG
ENST00000426902.5:c.322+143_322+144insCTG ENSP00000395636.1:n.322+143_322+144insCTG
ENST00000593731.1:c.322+143_322+144insCTG ENSP00000471914.1:n.322+143_322+144insCTG
ENST00000617130.4:c.322+143_322+144insCTG ENSP00000477864.1:n.322+143_322+144insCTG
ENST00000617642.1:c.322+143_322+144insCTG ENSP00000484714.1:n.322+143_322+144insCTG
NM_005027.3:c.322+143_322+144insCTG NP_005018.1:n.322+143_322+144insCTG
NR_073517.1:n.862+143_862+144insCTG
NM_005027.4:c.322+143_322+144insCTG MANE Select NP_005018.2:n.322+143_322+144insCTG
NR_073517.2:n.877+143_877+144insCTG
NR_162071.1:n.877+143_877+144insCTG
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