Canonical Allele Identifier: CA7608459

Gene: PPIB SNX22

Linked Data

• dbSNP Id: rs763594413
• ExAC: 15:64448891 TGCCCAGTAGTA / T
• gnomAD v2: 15-64448891-TGCCCAGTAGTA-T
• gnomAD v4: 15-64156692-TGCCCAGTAGTA-T
• MyVariant Identifiers: chr15:g.64448892_64448902del (hg19) ; chr15:g.64156693_64156703del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156697_64156707del , CM000677.2:g.64156697_64156707del	GRCh38
NC_000015.9:g.64448896_64448906del , CM000677.1:g.64448896_64448906del	GRCh37
NC_000015.8:g.62235949_62235959del	NCBI36
NG_012979.1:g.11453_11463del , LRG_10:g.11453_11463del
NG_033071.1:g.9981_9991del

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.528+22_528+32del (PPIB) MANE Select	ENSP00000300026.4:n.528+22_528+32del
ENST00000325881.9:c.*2189_*2199del (SNX22) MANE Select	ENSP00000323435.4:n.*2189_*2199del
ENST00000561048.2:n.3755+22_3755+32del (PPIB)
ENST00000680158.1:c.*201+22_*201+32del (PPIB)	ENSP00000504873.1:n.*201+22_*201+32del
ENST00000680343.1:n.482+22_482+32del (PPIB)
ENST00000681397.1:c.528+22_528+32del (PPIB)	ENSP00000506584.1:n.528+22_528+32del
ENST00000681658.1:c.423+22_423+32del (PPIB)	ENSP00000505431.1:n.423+22_423+32del
ENST00000300026.3:c.528+22_528+32del (PPIB)	ENSP00000300026.3:n.528+22_528+32del
ENST00000325881.8:c.*2189_*2199del (SNX22)	ENSP00000323435.4:n.*2189_*2199del
ENST00000557789.5:n.2929_2939del (SNX22)
ENST00000560997.1:n.2584_2594del (SNX22)
NM_000942.4:c.528+22_528+32del , LRG_10t1:c.528+22_528+32del (PPIB)	NP_000933.1:n.528+22_528+32del
NM_024798.2:c.*2189_*2199del (SNX22)	NP_079074.2:n.*2189_*2199del
NR_073534.1:n.2877_2887del (SNX22)
XM_017022581.1:c.*2189_*2199del (SNX22)	XP_016878070.1:n.*2189_*2199del
NM_024798.3:c.*2189_*2199del (SNX22) MANE Select	NP_079074.2:n.*2189_*2199del
NM_000942.5:c.528+22_528+32del (PPIB) MANE Select	NP_000933.1:n.528+22_528+32del
NR_073534.2:n.2863_2873del (SNX22)