Canonical Allele Identifier: CA490812221

Gene: PPIB SNX22

Linked Data

• MyVariant Identifiers: chr15:g.64449016_64449017insGCGACCCA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156817_64156818insGCGACCCA , CM000677.2:g.64156817_64156818insGCGACCCA	GRCh38
NC_000015.9:g.64449016_64449017insGCGACCCA , CM000677.1:g.64449016_64449017insGCGACCCA	GRCh37
NC_000015.8:g.62236069_62236070insGCGACCCA	NCBI36
NG_012979.1:g.11338_11339insTGGGTCGC , LRG_10:g.11338_11339insTGGGTCGC
NG_033071.1:g.10101_10102insGCGACCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.435_436insTGGGTCGC (PPIB) MANE Select	ENSP00000300026.4:p.Asp146TrpfsTer20
ENST00000325881.9:c.*2309_*2310insGCGACCCA (SNX22) MANE Select	ENSP00000323435.4:n.*2309_*2310insGCGACCCA
ENST00000561048.2:n.3662_3663insTGGGTCGC (PPIB)
ENST00000680158.1:c.*108_*109insTGGGTCGC (PPIB)	ENSP00000504873.1:n.*108_*109insTGGGTCGC
ENST00000680343.1:n.389_390insTGGGTCGC (PPIB)
ENST00000681397.1:c.435_436insTGGGTCGC (PPIB)	ENSP00000506584.1:p.Asp146TrpfsTer20
ENST00000681658.1:c.330_331insTGGGTCGC (PPIB)	ENSP00000505431.1:p.Asp111TrpfsTer20
ENST00000300026.3:c.435_436insTGGGTCGC (PPIB)	ENSP00000300026.3:p.Asp146TrpfsTer20
ENST00000325881.8:c.*2309_*2310insGCGACCCA (SNX22)	ENSP00000323435.4:n.*2309_*2310insGCGACCCA
ENST00000557789.5:n.3049_3050insGCGACCCA (SNX22)
ENST00000558492.1:n.341_342insTGGGTCGC (PPIB)
ENST00000560997.1:n.2704_2705insGCGACCCA (SNX22)
NM_000942.4:c.435_436insTGGGTCGC , LRG_10t1:c.435_436insTGGGTCGC (PPIB)	NP_000933.1:p.Asp146TrpfsTer20
NM_024798.2:c.*2309_*2310insGCGACCCA (SNX22)	NP_079074.2:n.*2309_*2310insGCGACCCA
NR_073534.1:n.2997_2998insGCGACCCA (SNX22)
XM_017022581.1:c.*2309_*2310insGCGACCCA (SNX22)	XP_016878070.1:n.*2309_*2310insGCGACCCA
NM_024798.3:c.*2309_*2310insGCGACCCA (SNX22) MANE Select	NP_079074.2:n.*2309_*2310insGCGACCCA
NM_000942.5:c.435_436insTGGGTCGC (PPIB) MANE Select	NP_000933.1:p.Asp146TrpfsTer20
NR_073534.2:n.2983_2984insGCGACCCA (SNX22)