Canonical Allele Identifier: CA2183002813

Gene: PPIB SNX22

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64157136_64157139delinsCAGA , CM000677.2:g.64157136_64157139delinsCAGA	GRCh38
NC_000015.9:g.64449335_64449338delinsCAGA , CM000677.1:g.64449335_64449338delinsCAGA	GRCh37
NC_000015.8:g.62236388_62236391delinsCAGA	NCBI36
NG_012979.1:g.11017_11020delinsTCTG , LRG_10:g.11017_11020delinsTCTG
NG_033071.1:g.10420_10423delinsCAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.344-230_344-227delinsTCTG (PPIB) MANE Select	ENSP00000300026.4:n.344-230_344-227delinsTCTG
ENST00000325881.9:c.*2628_*2631delinsCAGA (SNX22) MANE Select	ENSP00000323435.4:n.*2628_*2631delinsCAGA
ENST00000561048.2:n.3341_3344delinsTCTG (PPIB)
ENST00000680158.1:c.*17-230_*17-227delinsTCTG (PPIB)	ENSP00000504873.1:n.*17-230_*17-227delinsTCTG
ENST00000680343.1:n.298-230_298-227delinsTCTG (PPIB)
ENST00000681397.1:c.344-230_344-227delinsTCTG (PPIB)	ENSP00000506584.1:n.344-230_344-227delinsTCTG
ENST00000681658.1:c.239-230_239-227delinsTCTG (PPIB)	ENSP00000505431.1:n.239-230_239-227delinsTCTG
ENST00000300026.3:c.344-230_344-227delinsTCTG (PPIB)	ENSP00000300026.3:n.344-230_344-227delinsTCTG
ENST00000325881.8:c.*2628_*2631delinsCAGA (SNX22)	ENSP00000323435.4:n.*2628_*2631delinsCAGA
ENST00000557789.5:n.3368_3371delinsCAGA (SNX22)
ENST00000558492.1:n.250-230_250-227delinsTCTG (PPIB)
ENST00000560997.1:n.3023_3026delinsCAGA (SNX22)
NM_000942.4:c.344-230_344-227delinsTCTG , LRG_10t1:c.344-230_344-227delinsTCTG (PPIB)	NP_000933.1:n.344-230_344-227delinsTCTG
NM_024798.2:c.*2628_*2631delinsCAGA (SNX22)	NP_079074.2:n.*2628_*2631delinsCAGA
NR_073534.1:n.3316_3319delinsCAGA (SNX22)
XM_017022581.1:c.*2628_*2631delinsCAGA (SNX22)	XP_016878070.1:n.*2628_*2631delinsCAGA
NM_024798.3:c.*2628_*2631delinsCAGA (SNX22) MANE Select	NP_079074.2:n.*2628_*2631delinsCAGA
NM_000942.5:c.344-230_344-227delinsTCTG (PPIB) MANE Select	NP_000933.1:n.344-230_344-227delinsTCTG
NR_073534.2:n.3302_3305delinsCAGA (SNX22)