Canonical Allele Identifier: CA2628931259

Gene: PPIB SNX22

Linked Data

• gnomAD v4: 15-64157159-A-AGTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64157160_64157163dup , CM000677.2:g.64157160_64157163dup	GRCh38
NC_000015.9:g.64449359_64449362dup , CM000677.1:g.64449359_64449362dup	GRCh37
NC_000015.8:g.62236412_62236415dup	NCBI36
NG_012979.1:g.10993_10996dup , LRG_10:g.10993_10996dup
NG_033071.1:g.10444_10447dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.344-254_344-251dup (PPIB) MANE Select	ENSP00000300026.4:n.344-254_344-251dup
ENST00000325881.9:c.*2652_*2655dup (SNX22) MANE Select	ENSP00000323435.4:n.*2652_*2655dup
ENST00000561048.2:n.3317_3320dup (PPIB)
ENST00000680158.1:c.*17-254_*17-251dup (PPIB)	ENSP00000504873.1:n.*17-254_*17-251dup
ENST00000680343.1:n.298-254_298-251dup (PPIB)
ENST00000681397.1:c.344-254_344-251dup (PPIB)	ENSP00000506584.1:n.344-254_344-251dup
ENST00000681658.1:c.239-254_239-251dup (PPIB)	ENSP00000505431.1:n.239-254_239-251dup
ENST00000300026.3:c.344-254_344-251dup (PPIB)	ENSP00000300026.3:n.344-254_344-251dup
ENST00000325881.8:c.*2652_*2655dup (SNX22)	ENSP00000323435.4:n.*2652_*2655dup
ENST00000557789.5:n.3392_3395dup (SNX22)
ENST00000558492.1:n.250-254_250-251dup (PPIB)
ENST00000560997.1:n.3047_3050dup (SNX22)
NM_000942.4:c.344-254_344-251dup , LRG_10t1:c.344-254_344-251dup (PPIB)	NP_000933.1:n.344-254_344-251dup
NM_024798.2:c.*2652_*2655dup (SNX22)	NP_079074.2:n.*2652_*2655dup
NR_073534.1:n.3340_3343dup (SNX22)
XM_017022581.1:c.*2652_*2655dup (SNX22)	XP_016878070.1:n.*2652_*2655dup
NM_024798.3:c.*2652_*2655dup (SNX22) MANE Select	NP_079074.2:n.*2652_*2655dup
NM_000942.5:c.344-254_344-251dup (PPIB) MANE Select	NP_000933.1:n.344-254_344-251dup
NR_073534.2:n.3326_3329dup (SNX22)