Canonical Allele Identifier: CA2804477251

Gene: PPIB SNX22

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64157126_64157127insTTTGGC , CM000677.2:g.64157126_64157127insTTTGGC	GRCh38
NC_000015.9:g.64449325_64449326insTTTGGC , CM000677.1:g.64449325_64449326insTTTGGC	GRCh37
NC_000015.8:g.62236378_62236379insTTTGGC	NCBI36
NG_012979.1:g.11029_11030insGCCAAA , LRG_10:g.11029_11030insGCCAAA
NG_033071.1:g.10410_10411insTTTGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.344-218_344-217insGCCAAA (PPIB) MANE Select	ENSP00000300026.4:n.344-218_344-217insGCCAAA
ENST00000325881.9:c.*2618_*2619insTTTGGC (SNX22) MANE Select	ENSP00000323435.4:n.*2618_*2619insTTTGGC
ENST00000561048.2:n.3353_3354insGCCAAA (PPIB)
ENST00000680158.1:c.*17-218_*17-217insGCCAAA (PPIB)	ENSP00000504873.1:n.*17-218_*17-217insGCCAAA
ENST00000680343.1:n.298-218_298-217insGCCAAA (PPIB)
ENST00000681397.1:c.344-218_344-217insGCCAAA (PPIB)	ENSP00000506584.1:n.344-218_344-217insGCCAAA
ENST00000681658.1:c.239-218_239-217insGCCAAA (PPIB)	ENSP00000505431.1:n.239-218_239-217insGCCAAA
ENST00000300026.3:c.344-218_344-217insGCCAAA (PPIB)	ENSP00000300026.3:n.344-218_344-217insGCCAAA
ENST00000325881.8:c.*2618_*2619insTTTGGC (SNX22)	ENSP00000323435.4:n.*2618_*2619insTTTGGC
ENST00000557789.5:n.3358_3359insTTTGGC (SNX22)
ENST00000558492.1:n.250-218_250-217insGCCAAA (PPIB)
ENST00000560997.1:n.3013_3014insTTTGGC (SNX22)
NM_000942.4:c.344-218_344-217insGCCAAA , LRG_10t1:c.344-218_344-217insGCCAAA (PPIB)	NP_000933.1:n.344-218_344-217insGCCAAA
NM_024798.2:c.*2618_*2619insTTTGGC (SNX22)	NP_079074.2:n.*2618_*2619insTTTGGC
NR_073534.1:n.3306_3307insTTTGGC (SNX22)
XM_017022581.1:c.*2618_*2619insTTTGGC (SNX22)	XP_016878070.1:n.*2618_*2619insTTTGGC
NM_024798.3:c.*2618_*2619insTTTGGC (SNX22) MANE Select	NP_079074.2:n.*2618_*2619insTTTGGC
NM_000942.5:c.344-218_344-217insGCCAAA (PPIB) MANE Select	NP_000933.1:n.344-218_344-217insGCCAAA
NR_073534.2:n.3292_3293insTTTGGC (SNX22)