Canonical Allele Identifier: CA2183002589

Gene: PPIB SNX22

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156687_64156688delinsAG , CM000677.2:g.64156687_64156688delinsAG	GRCh38
NC_000015.9:g.64448886_64448887delinsAG , CM000677.1:g.64448886_64448887delinsAG	GRCh37
NC_000015.8:g.62235939_62235940delinsAG	NCBI36
NG_012979.1:g.11468_11469delinsCT , LRG_10:g.11468_11469delinsCT
NG_033071.1:g.9971_9972delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.528+37_528+38delinsCT (PPIB) MANE Select	ENSP00000300026.4:n.528+37_528+38delinsCT
ENST00000325881.9:c.*2179_*2180delinsAG (SNX22) MANE Select	ENSP00000323435.4:n.*2179_*2180delinsAG
ENST00000561048.2:n.3755+37_3755+38delinsCT (PPIB)
ENST00000680158.1:c.*201+37_*201+38delinsCT (PPIB)	ENSP00000504873.1:n.*201+37_*201+38delinsCT
ENST00000680343.1:n.482+37_482+38delinsCT (PPIB)
ENST00000681397.1:c.528+37_528+38delinsCT (PPIB)	ENSP00000506584.1:n.528+37_528+38delinsCT
ENST00000681658.1:c.423+37_423+38delinsCT (PPIB)	ENSP00000505431.1:n.423+37_423+38delinsCT
ENST00000300026.3:c.528+37_528+38delinsCT (PPIB)	ENSP00000300026.3:n.528+37_528+38delinsCT
ENST00000325881.8:c.*2179_*2180delinsAG (SNX22)	ENSP00000323435.4:n.*2179_*2180delinsAG
ENST00000557789.5:n.2919_2920delinsAG (SNX22)
ENST00000560997.1:n.2574_2575delinsAG (SNX22)
NM_000942.4:c.528+37_528+38delinsCT , LRG_10t1:c.528+37_528+38delinsCT (PPIB)	NP_000933.1:n.528+37_528+38delinsCT
NM_024798.2:c.*2179_*2180delinsAG (SNX22)	NP_079074.2:n.*2179_*2180delinsAG
NR_073534.1:n.2867_2868delinsAG (SNX22)
XM_017022581.1:c.*2179_*2180delinsAG (SNX22)	XP_016878070.1:n.*2179_*2180delinsAG
NM_024798.3:c.*2179_*2180delinsAG (SNX22) MANE Select	NP_079074.2:n.*2179_*2180delinsAG
NM_000942.5:c.528+37_528+38delinsCT (PPIB) MANE Select	NP_000933.1:n.528+37_528+38delinsCT
NR_073534.2:n.2853_2854delinsAG (SNX22)