Canonical Allele Identifier: CA2628930288

Gene: PPIB SNX22

Linked Data

• gnomAD v4: 15-64156702-T-TAGC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156703_64156705dup , CM000677.2:g.64156703_64156705dup	GRCh38
NC_000015.9:g.64448902_64448904dup , CM000677.1:g.64448902_64448904dup	GRCh37
NC_000015.8:g.62235955_62235957dup	NCBI36
NG_012979.1:g.11451_11453dup , LRG_10:g.11451_11453dup
NG_033071.1:g.9987_9989dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.528+20_528+22dup (PPIB) MANE Select	ENSP00000300026.4:n.528+20_528+22dup
ENST00000325881.9:c.*2195_*2197dup (SNX22) MANE Select	ENSP00000323435.4:n.*2195_*2197dup
ENST00000561048.2:n.3755+20_3755+22dup (PPIB)
ENST00000680158.1:c.*201+20_*201+22dup (PPIB)	ENSP00000504873.1:n.*201+20_*201+22dup
ENST00000680343.1:n.482+20_482+22dup (PPIB)
ENST00000681397.1:c.528+20_528+22dup (PPIB)	ENSP00000506584.1:n.528+20_528+22dup
ENST00000681658.1:c.423+20_423+22dup (PPIB)	ENSP00000505431.1:n.423+20_423+22dup
ENST00000300026.3:c.528+20_528+22dup (PPIB)	ENSP00000300026.3:n.528+20_528+22dup
ENST00000325881.8:c.*2195_*2197dup (SNX22)	ENSP00000323435.4:n.*2195_*2197dup
ENST00000557789.5:n.2935_2937dup (SNX22)
ENST00000560997.1:n.2590_2592dup (SNX22)
NM_000942.4:c.528+20_528+22dup , LRG_10t1:c.528+20_528+22dup (PPIB)	NP_000933.1:n.528+20_528+22dup
NM_024798.2:c.*2195_*2197dup (SNX22)	NP_079074.2:n.*2195_*2197dup
NR_073534.1:n.2883_2885dup (SNX22)
XM_017022581.1:c.*2195_*2197dup (SNX22)	XP_016878070.1:n.*2195_*2197dup
NM_024798.3:c.*2195_*2197dup (SNX22) MANE Select	NP_079074.2:n.*2195_*2197dup
NM_000942.5:c.528+20_528+22dup (PPIB) MANE Select	NP_000933.1:n.528+20_528+22dup
NR_073534.2:n.2869_2871dup (SNX22)