Canonical Allele Identifier: CA2581998426
Gene: PIK3R2 HGNC NCBI

Linked Data

gnomAD v3: 19-18156137-CGGCCCTCGCCCACGG-C
gnomAD v4: 19-18156137-CGGCCCTCGCCCACGG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18156143_18156157del , CM000681.2:g.18156143_18156157del GRCh38
NC_000019.9:g.18266953_18266967del , CM000681.1:g.18266953_18266967del GRCh37
NC_000019.8:g.18127953_18127967del NCBI36
NG_033010.1:g.7966_7980del
NG_033010.2:g.7966_7980del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222254.13:c.264_278del MANE Select ENSP00000222254.6:p.Arg89_Pro93del
ENST00000617130.5:c.264_278del ENSP00000477864.2:p.Arg89_Pro93del
ENST00000617642.2:c.264_278del ENSP00000484714.2:p.Arg89_Pro93del
ENST00000222254.12:c.264_278del ENSP00000222254.6:p.Arg89_Pro93del
ENST00000426902.5:c.264_278del ENSP00000395636.1:p.Arg89_Pro93del
ENST00000593731.1:c.264_278del ENSP00000471914.1:p.Arg89_Pro93del
ENST00000617130.4:c.264_278del ENSP00000477864.1:p.Arg89_Pro93del
ENST00000617642.1:c.264_278del ENSP00000484714.1:p.Arg89_Pro93del
NM_005027.3:c.264_278del NP_005018.1:p.Arg89_Pro93del
NR_073517.1:n.804_818del
NM_005027.4:c.264_278del MANE Select NP_005018.2:p.Arg89_Pro93del
NR_073517.2:n.819_833del
NR_162071.1:n.819_833del
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