Canonical Allele Identifier: CA2628931156

Gene: PPIB SNX22

Linked Data

• gnomAD v4: 15-64157094-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64157095_64157096insTC , CM000677.2:g.64157095_64157096insTC	GRCh38
NC_000015.9:g.64449294_64449295insTC , CM000677.1:g.64449294_64449295insTC	GRCh37
NC_000015.8:g.62236347_62236348insTC	NCBI36
NG_012979.1:g.11061_11062insAG , LRG_10:g.11061_11062insAG
NG_033071.1:g.10379_10380insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.344-186_344-185insAG (PPIB) MANE Select	ENSP00000300026.4:n.344-186_344-185insAG
ENST00000325881.9:c.*2587_*2588insTC (SNX22) MANE Select	ENSP00000323435.4:n.*2587_*2588insTC
ENST00000561048.2:n.3385_3386insAG (PPIB)
ENST00000680158.1:c.*17-186_*17-185insAG (PPIB)	ENSP00000504873.1:n.*17-186_*17-185insAG
ENST00000680343.1:n.298-186_298-185insAG (PPIB)
ENST00000681397.1:c.344-186_344-185insAG (PPIB)	ENSP00000506584.1:n.344-186_344-185insAG
ENST00000681658.1:c.239-186_239-185insAG (PPIB)	ENSP00000505431.1:n.239-186_239-185insAG
ENST00000300026.3:c.344-186_344-185insAG (PPIB)	ENSP00000300026.3:n.344-186_344-185insAG
ENST00000325881.8:c.*2587_*2588insTC (SNX22)	ENSP00000323435.4:n.*2587_*2588insTC
ENST00000557789.5:n.3327_3328insTC (SNX22)
ENST00000558492.1:n.250-186_250-185insAG (PPIB)
ENST00000560997.1:n.2982_2983insTC (SNX22)
NM_000942.4:c.344-186_344-185insAG , LRG_10t1:c.344-186_344-185insAG (PPIB)	NP_000933.1:n.344-186_344-185insAG
NM_024798.2:c.*2587_*2588insTC (SNX22)	NP_079074.2:n.*2587_*2588insTC
NR_073534.1:n.3275_3276insTC (SNX22)
XM_017022581.1:c.*2587_*2588insTC (SNX22)	XP_016878070.1:n.*2587_*2588insTC
NM_024798.3:c.*2587_*2588insTC (SNX22) MANE Select	NP_079074.2:n.*2587_*2588insTC
NM_000942.5:c.344-186_344-185insAG (PPIB) MANE Select	NP_000933.1:n.344-186_344-185insAG
NR_073534.2:n.3261_3262insTC (SNX22)