Canonical Allele Identifier: CA490812220

Gene: PPIB SNX22

Linked Data

• MyVariant Identifiers: chr15:g.64449014_64449015insC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156815_64156816insC , CM000677.2:g.64156815_64156816insC	GRCh38
NC_000015.9:g.64449014_64449015insC , CM000677.1:g.64449014_64449015insC	GRCh37
NC_000015.8:g.62236067_62236068insC	NCBI36
NG_012979.1:g.11340_11341insG , LRG_10:g.11340_11341insG
NG_033071.1:g.10099_10100insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.437_438insG (PPIB) MANE Select	ENSP00000300026.4:p.Asp146GlufsTer?
ENST00000325881.9:c.*2307_*2308insC (SNX22) MANE Select	ENSP00000323435.4:n.*2307_*2308insC
ENST00000561048.2:n.3664_3665insG (PPIB)
ENST00000680158.1:c.*110_*111insG (PPIB)	ENSP00000504873.1:n.*110_*111insG
ENST00000680343.1:n.391_392insG (PPIB)
ENST00000681397.1:c.437_438insG (PPIB)	ENSP00000506584.1:p.Asp146GlufsTer?
ENST00000681658.1:c.332_333insG (PPIB)	ENSP00000505431.1:p.Asp111GlufsTer?
ENST00000300026.3:c.437_438insG (PPIB)	ENSP00000300026.3:p.Asp146GlufsTer?
ENST00000325881.8:c.*2307_*2308insC (SNX22)	ENSP00000323435.4:n.*2307_*2308insC
ENST00000557789.5:n.3047_3048insC (SNX22)
ENST00000558492.1:n.343_344insG (PPIB)
ENST00000560997.1:n.2702_2703insC (SNX22)
NM_000942.4:c.437_438insG , LRG_10t1:c.437_438insG (PPIB)	NP_000933.1:p.Asp146GlufsTer?
NM_024798.2:c.*2307_*2308insC (SNX22)	NP_079074.2:n.*2307_*2308insC
NR_073534.1:n.2995_2996insC (SNX22)
XM_017022581.1:c.*2307_*2308insC (SNX22)	XP_016878070.1:n.*2307_*2308insC
NM_024798.3:c.*2307_*2308insC (SNX22) MANE Select	NP_079074.2:n.*2307_*2308insC
NM_000942.5:c.437_438insG (PPIB) MANE Select	NP_000933.1:p.Asp146GlufsTer?
NR_073534.2:n.2981_2982insC (SNX22)