Canonical Allele Identifier: CA271410112

Gene: PPIB SNX22

Linked Data

• dbSNP Id: rs878892376
• MyVariant Identifiers: chr15:g.64448922_64448923insT (hg19) ; chr15:g.64156723_64156724insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156723_64156724insT , CM000677.2:g.64156723_64156724insT	GRCh38
NC_000015.9:g.64448922_64448923insT , CM000677.1:g.64448922_64448923insT	GRCh37
NC_000015.8:g.62235975_62235976insT	NCBI36
NG_012979.1:g.11432_11433insA , LRG_10:g.11432_11433insA
NG_033071.1:g.10007_10008insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.528+1_528+2insA (PPIB) MANE Select	ENSP00000300026.4:n.528+1_528+2insA
ENST00000325881.9:c.*2215_*2216insT (SNX22) MANE Select	ENSP00000323435.4:n.*2215_*2216insT
ENST00000561048.2:n.3755+1_3755+2insA (PPIB)
ENST00000680158.1:c.*201+1_*201+2insA (PPIB)	ENSP00000504873.1:n.*201+1_*201+2insA
ENST00000680343.1:n.482+1_482+2insA (PPIB)
ENST00000681397.1:c.528+1_528+2insA (PPIB)	ENSP00000506584.1:n.528+1_528+2insA
ENST00000681658.1:c.423+1_423+2insA (PPIB)	ENSP00000505431.1:n.423+1_423+2insA
ENST00000300026.3:c.528+1_528+2insA (PPIB)	ENSP00000300026.3:n.528+1_528+2insA
ENST00000325881.8:c.*2215_*2216insT (SNX22)	ENSP00000323435.4:n.*2215_*2216insT
ENST00000557789.5:n.2955_2956insT (SNX22)
ENST00000560997.1:n.2610_2611insT (SNX22)
NM_000942.4:c.528+1_528+2insA , LRG_10t1:c.528+1_528+2insA (PPIB)	NP_000933.1:n.528+1_528+2insA
NM_024798.2:c.*2215_*2216insT (SNX22)	NP_079074.2:n.*2215_*2216insT
NR_073534.1:n.2903_2904insT (SNX22)
XM_017022581.1:c.*2215_*2216insT (SNX22)	XP_016878070.1:n.*2215_*2216insT
NM_024798.3:c.*2215_*2216insT (SNX22) MANE Select	NP_079074.2:n.*2215_*2216insT
NM_000942.5:c.528+1_528+2insA (PPIB) MANE Select	NP_000933.1:n.528+1_528+2insA
NR_073534.2:n.2889_2890insT (SNX22)