Canonical Allele Identifier: CA2628931166

Gene: PPIB SNX22

Linked Data

• gnomAD v4: 15-64157099-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64157102_64157103dup , CM000677.2:g.64157102_64157103dup	GRCh38
NC_000015.9:g.64449301_64449302dup , CM000677.1:g.64449301_64449302dup	GRCh37
NC_000015.8:g.62236354_62236355dup	NCBI36
NG_012979.1:g.11055_11056dup , LRG_10:g.11055_11056dup
NG_033071.1:g.10386_10387dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.344-192_344-191dup (PPIB) MANE Select	ENSP00000300026.4:n.344-192_344-191dup
ENST00000325881.9:c.*2594_*2595dup (SNX22) MANE Select	ENSP00000323435.4:n.*2594_*2595dup
ENST00000561048.2:n.3379_3380dup (PPIB)
ENST00000680158.1:c.*17-192_*17-191dup (PPIB)	ENSP00000504873.1:n.*17-192_*17-191dup
ENST00000680343.1:n.298-192_298-191dup (PPIB)
ENST00000681397.1:c.344-192_344-191dup (PPIB)	ENSP00000506584.1:n.344-192_344-191dup
ENST00000681658.1:c.239-192_239-191dup (PPIB)	ENSP00000505431.1:n.239-192_239-191dup
ENST00000300026.3:c.344-192_344-191dup (PPIB)	ENSP00000300026.3:n.344-192_344-191dup
ENST00000325881.8:c.*2594_*2595dup (SNX22)	ENSP00000323435.4:n.*2594_*2595dup
ENST00000557789.5:n.3334_3335dup (SNX22)
ENST00000558492.1:n.250-192_250-191dup (PPIB)
ENST00000560997.1:n.2989_2990dup (SNX22)
NM_000942.4:c.344-192_344-191dup , LRG_10t1:c.344-192_344-191dup (PPIB)	NP_000933.1:n.344-192_344-191dup
NM_024798.2:c.*2594_*2595dup (SNX22)	NP_079074.2:n.*2594_*2595dup
NR_073534.1:n.3282_3283dup (SNX22)
XM_017022581.1:c.*2594_*2595dup (SNX22)	XP_016878070.1:n.*2594_*2595dup
NM_024798.3:c.*2594_*2595dup (SNX22) MANE Select	NP_079074.2:n.*2594_*2595dup
NM_000942.5:c.344-192_344-191dup (PPIB) MANE Select	NP_000933.1:n.344-192_344-191dup
NR_073534.2:n.3268_3269dup (SNX22)