Canonical Allele Identifier: CA2804477252

Gene: PPIB SNX22

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64157128_64157129insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG , CM000677.2:g.64157128_64157129insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG	GRCh38
NC_000015.9:g.64449327_64449328insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG , CM000677.1:g.64449327_64449328insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG	GRCh37
NC_000015.8:g.62236380_62236381insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG	NCBI36
NG_012979.1:g.11027_11028insCTTCCACAACTCACCATGCCCTCTAGAACT , LRG_10:g.11027_11028insCTTCCACAACTCACCATGCCCTCTAGAACT
NG_033071.1:g.10412_10413insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.344-220_344-219insCTTCCACAACTCACCATGCCCTCTAGAACT (PPIB) MANE Select	ENSP00000300026.4:n.344-220_344-219insCTTCCACAACTCACCATGCCCTC...
ENST00000325881.9:c.*2620_*2621insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG (SNX22) MANE Select	ENSP00000323435.4:n.*2620_*2621insAGTTCTAGAGGGCATGGTGAGTTGTGG...
ENST00000561048.2:n.3351_3352insCTTCCACAACTCACCATGCCCTCTAGAACT (PPIB)
ENST00000680158.1:c.*17-220_*17-219insCTTCCACAACTCACCATGCCCTCTAGAACT (PPIB)	ENSP00000504873.1:n.*17-220_*17-219insCTTCCACAACTCACCATGCCCTC...
ENST00000680343.1:n.298-220_298-219insCTTCCACAACTCACCATGCCCTCTAGAACT (PPIB)
ENST00000681397.1:c.344-220_344-219insCTTCCACAACTCACCATGCCCTCTAGAACT (PPIB)	ENSP00000506584.1:n.344-220_344-219insCTTCCACAACTCACCATGCCCTC...
ENST00000681658.1:c.239-220_239-219insCTTCCACAACTCACCATGCCCTCTAGAACT (PPIB)	ENSP00000505431.1:n.239-220_239-219insCTTCCACAACTCACCATGCCCTC...
ENST00000300026.3:c.344-220_344-219insCTTCCACAACTCACCATGCCCTCTAGAACT (PPIB)	ENSP00000300026.3:n.344-220_344-219insCTTCCACAACTCACCATGCCCTC...
ENST00000325881.8:c.*2620_*2621insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG (SNX22)	ENSP00000323435.4:n.*2620_*2621insAGTTCTAGAGGGCATGGTGAGTTGTGG...
ENST00000557789.5:n.3360_3361insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG (SNX22)
ENST00000558492.1:n.250-220_250-219insCTTCCACAACTCACCATGCCCTCTAGAACT (PPIB)
ENST00000560997.1:n.3015_3016insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG (SNX22)
NM_000942.4:c.344-220_344-219insCTTCCACAACTCACCATGCCCTCTAGAACT , LRG_10t1:c.344-220_344-219insCTTCCACAACTCACCATGCCCTCTAGAACT (PPIB)	NP_000933.1:n.344-220_344-219insCTTCCACAACTCACCATGCCCTCTAGAAC...
NM_024798.2:c.*2620_*2621insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG (SNX22)	NP_079074.2:n.*2620_*2621insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG
NR_073534.1:n.3308_3309insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG (SNX22)
XM_017022581.1:c.*2620_*2621insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG (SNX22)	XP_016878070.1:n.*2620_*2621insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG...
NM_024798.3:c.*2620_*2621insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG (SNX22) MANE Select	NP_079074.2:n.*2620_*2621insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG
NM_000942.5:c.344-220_344-219insCTTCCACAACTCACCATGCCCTCTAGAACT (PPIB) MANE Select	NP_000933.1:n.344-220_344-219insCTTCCACAACTCACCATGCCCTCTAGAAC...
NR_073534.2:n.3294_3295insAGTTCTAGAGGGCATGGTGAGTTGTGGAAG (SNX22)