Canonical Allele Identifier: CA2628930219

Gene: PPIB SNX22

Linked Data

• gnomAD v4: 15-64156639-A-ATGGACACATGGAGCTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156642_64156658dup , CM000677.2:g.64156642_64156658dup	GRCh38
NC_000015.9:g.64448841_64448857dup , CM000677.1:g.64448841_64448857dup	GRCh37
NC_000015.8:g.62235894_62235910dup	NCBI36
NG_012979.1:g.11500_11516dup , LRG_10:g.11500_11516dup
NG_033071.1:g.9926_9942dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.528+69_528+85dup (PPIB) MANE Select	ENSP00000300026.4:n.528+69_528+85dup
ENST00000325881.9:c.*2134_*2150dup (SNX22) MANE Select	ENSP00000323435.4:n.*2134_*2150dup
ENST00000561048.2:n.3755+69_3755+85dup (PPIB)
ENST00000680158.1:c.*201+69_*201+85dup (PPIB)	ENSP00000504873.1:n.*201+69_*201+85dup
ENST00000680343.1:n.482+69_482+85dup (PPIB)
ENST00000681397.1:c.528+69_528+85dup (PPIB)	ENSP00000506584.1:n.528+69_528+85dup
ENST00000681658.1:c.423+69_423+85dup (PPIB)	ENSP00000505431.1:n.423+69_423+85dup
ENST00000300026.3:c.528+69_528+85dup (PPIB)	ENSP00000300026.3:n.528+69_528+85dup
ENST00000325881.8:c.*2134_*2150dup (SNX22)	ENSP00000323435.4:n.*2134_*2150dup
ENST00000557789.5:n.2874_2890dup (SNX22)
ENST00000560997.1:n.2529_2545dup (SNX22)
NM_000942.4:c.528+69_528+85dup , LRG_10t1:c.528+69_528+85dup (PPIB)	NP_000933.1:n.528+69_528+85dup
NM_024798.2:c.*2134_*2150dup (SNX22)	NP_079074.2:n.*2134_*2150dup
NR_073534.1:n.2822_2838dup (SNX22)
XM_017022581.1:c.*2134_*2150dup (SNX22)	XP_016878070.1:n.*2134_*2150dup
NM_024798.3:c.*2134_*2150dup (SNX22) MANE Select	NP_079074.2:n.*2134_*2150dup
NM_000942.5:c.528+69_528+85dup (PPIB) MANE Select	NP_000933.1:n.528+69_528+85dup
NR_073534.2:n.2808_2824dup (SNX22)