Canonical Allele Identifier: CA2559597047

Gene: PPIB SNX22

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156819_64156820insGCCCATGCGCT , CM000677.2:g.64156819_64156820insGCCCATGCGCT	GRCh38
NC_000015.9:g.64449018_64449019insGCCCATGCGCT , CM000677.1:g.64449018_64449019insGCCCATGCGCT	GRCh37
NC_000015.8:g.62236071_62236072insGCCCATGCGCT	NCBI36
NG_012979.1:g.11337_11338insGCGCATGGGCA , LRG_10:g.11337_11338insGCGCATGGGCA
NG_033071.1:g.10103_10104insGCCCATGCGCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.434_435insGCGCATGGGCA (PPIB) MANE Select	ENSP00000300026.4:p.Asp146ArgfsTer21
ENST00000325881.9:c.*2311_*2312insGCCCATGCGCT (SNX22) MANE Select	ENSP00000323435.4:n.*2311_*2312insGCCCATGCGCT
ENST00000561048.2:n.3661_3662insGCGCATGGGCA (PPIB)
ENST00000680158.1:c.*107_*108insGCGCATGGGCA (PPIB)	ENSP00000504873.1:n.*107_*108insGCGCATGGGCA
ENST00000680343.1:n.388_389insGCGCATGGGCA (PPIB)
ENST00000681397.1:c.434_435insGCGCATGGGCA (PPIB)	ENSP00000506584.1:p.Asp146ArgfsTer21
ENST00000681658.1:c.329_330insGCGCATGGGCA (PPIB)	ENSP00000505431.1:p.Asp111ArgfsTer21
ENST00000300026.3:c.434_435insGCGCATGGGCA (PPIB)	ENSP00000300026.3:p.Asp146ArgfsTer21
ENST00000325881.8:c.*2311_*2312insGCCCATGCGCT (SNX22)	ENSP00000323435.4:n.*2311_*2312insGCCCATGCGCT
ENST00000557789.5:n.3051_3052insGCCCATGCGCT (SNX22)
ENST00000558492.1:n.340_341insGCGCATGGGCA (PPIB)
ENST00000560997.1:n.2706_2707insGCCCATGCGCT (SNX22)
NM_000942.4:c.434_435insGCGCATGGGCA , LRG_10t1:c.434_435insGCGCATGGGCA (PPIB)	NP_000933.1:p.Asp146ArgfsTer21
NM_024798.2:c.*2311_*2312insGCCCATGCGCT (SNX22)	NP_079074.2:n.*2311_*2312insGCCCATGCGCT
NR_073534.1:n.2999_3000insGCCCATGCGCT (SNX22)
XM_017022581.1:c.*2311_*2312insGCCCATGCGCT (SNX22)	XP_016878070.1:n.*2311_*2312insGCCCATGCGCT
NM_024798.3:c.*2311_*2312insGCCCATGCGCT (SNX22) MANE Select	NP_079074.2:n.*2311_*2312insGCCCATGCGCT
NM_000942.5:c.434_435insGCGCATGGGCA (PPIB) MANE Select	NP_000933.1:p.Asp146ArgfsTer21
NR_073534.2:n.2985_2986insGCCCATGCGCT (SNX22)