Canonical Allele Identifier: CA2326211416
Gene: PIK3R2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156071_18156073delinsACG , CM000681.2:g.18156071_18156073delinsACG GRCh38
NC_000019.9:g.18266881_18266883delinsACG , CM000681.1:g.18266881_18266883delinsACG GRCh37
NC_000019.8:g.18127881_18127883delinsACG NCBI36
NG_033010.1:g.7894_7896delinsACG
NG_033010.2:g.7894_7896delinsACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.192_194delinsACG MANE Select ENSP00000222254.6:p.Thr64=
ENST00000617130.5:c.192_194delinsACG ENSP00000477864.2:p.Thr64=
ENST00000617642.2:c.192_194delinsACG ENSP00000484714.2:p.Thr64=
ENST00000222254.12:c.192_194delinsACG ENSP00000222254.6:p.Thr64=
ENST00000426902.5:c.192_194delinsACG ENSP00000395636.1:p.Thr64=
ENST00000593731.1:c.192_194delinsACG ENSP00000471914.1:p.Thr64=
ENST00000617130.4:c.192_194delinsACG ENSP00000477864.1:p.Thr64=
ENST00000617642.1:c.192_194delinsACG ENSP00000484714.1:p.Thr64=
NM_005027.3:c.192_194delinsACG NP_005018.1:p.Thr64=
NR_073517.1:n.732_734delinsACG
NM_005027.4:c.192_194delinsACG MANE Select NP_005018.2:p.Thr64=
NR_073517.2:n.747_749delinsACG
NR_162071.1:n.747_749delinsACG
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