Canonical Allele Identifier: CA2183002821

Gene: PPIB SNX22

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64157153_64157154delinsGA , CM000677.2:g.64157153_64157154delinsGA	GRCh38
NC_000015.9:g.64449352_64449353delinsGA , CM000677.1:g.64449352_64449353delinsGA	GRCh37
NC_000015.8:g.62236405_62236406delinsGA	NCBI36
NG_012979.1:g.11002_11003delinsTC , LRG_10:g.11002_11003delinsTC
NG_033071.1:g.10437_10438delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.344-245_344-244delinsTC (PPIB) MANE Select	ENSP00000300026.4:n.344-245_344-244delinsTC
ENST00000325881.9:c.*2645_*2646delinsGA (SNX22) MANE Select	ENSP00000323435.4:n.*2645_*2646delinsGA
ENST00000561048.2:n.3326_3327delinsTC (PPIB)
ENST00000680158.1:c.*17-245_*17-244delinsTC (PPIB)	ENSP00000504873.1:n.*17-245_*17-244delinsTC
ENST00000680343.1:n.298-245_298-244delinsTC (PPIB)
ENST00000681397.1:c.344-245_344-244delinsTC (PPIB)	ENSP00000506584.1:n.344-245_344-244delinsTC
ENST00000681658.1:c.239-245_239-244delinsTC (PPIB)	ENSP00000505431.1:n.239-245_239-244delinsTC
ENST00000300026.3:c.344-245_344-244delinsTC (PPIB)	ENSP00000300026.3:n.344-245_344-244delinsTC
ENST00000325881.8:c.*2645_*2646delinsGA (SNX22)	ENSP00000323435.4:n.*2645_*2646delinsGA
ENST00000557789.5:n.3385_3386delinsGA (SNX22)
ENST00000558492.1:n.250-245_250-244delinsTC (PPIB)
ENST00000560997.1:n.3040_3041delinsGA (SNX22)
NM_000942.4:c.344-245_344-244delinsTC , LRG_10t1:c.344-245_344-244delinsTC (PPIB)	NP_000933.1:n.344-245_344-244delinsTC
NM_024798.2:c.*2645_*2646delinsGA (SNX22)	NP_079074.2:n.*2645_*2646delinsGA
NR_073534.1:n.3333_3334delinsGA (SNX22)
XM_017022581.1:c.*2645_*2646delinsGA (SNX22)	XP_016878070.1:n.*2645_*2646delinsGA
NM_024798.3:c.*2645_*2646delinsGA (SNX22) MANE Select	NP_079074.2:n.*2645_*2646delinsGA
NM_000942.5:c.344-245_344-244delinsTC (PPIB) MANE Select	NP_000933.1:n.344-245_344-244delinsTC
NR_073534.2:n.3319_3320delinsGA (SNX22)