Canonical Allele Identifier: CA714832280

Gene: PPIB SNX22

Linked Data

• dbSNP Id: rs1358274687
• gnomAD v3: 15-64156679-C-CA
• gnomAD v4: 15-64156679-C-CA
• MyVariant Identifiers: chr15:g.64448878_64448879insA (hg19) ; chr15:g.64156679_64156680insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156679_64156680insA , CM000677.2:g.64156679_64156680insA	GRCh38
NC_000015.9:g.64448878_64448879insA , CM000677.1:g.64448878_64448879insA	GRCh37
NC_000015.8:g.62235931_62235932insA	NCBI36
NG_012979.1:g.11476_11477insT , LRG_10:g.11476_11477insT
NG_033071.1:g.9963_9964insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.528+45_528+46insT (PPIB) MANE Select	ENSP00000300026.4:n.528+45_528+46insT
ENST00000325881.9:c.*2171_*2172insA (SNX22) MANE Select	ENSP00000323435.4:n.*2171_*2172insA
ENST00000561048.2:n.3755+45_3755+46insT (PPIB)
ENST00000680158.1:c.*201+45_*201+46insT (PPIB)	ENSP00000504873.1:n.*201+45_*201+46insT
ENST00000680343.1:n.482+45_482+46insT (PPIB)
ENST00000681397.1:c.528+45_528+46insT (PPIB)	ENSP00000506584.1:n.528+45_528+46insT
ENST00000681658.1:c.423+45_423+46insT (PPIB)	ENSP00000505431.1:n.423+45_423+46insT
ENST00000300026.3:c.528+45_528+46insT (PPIB)	ENSP00000300026.3:n.528+45_528+46insT
ENST00000325881.8:c.*2171_*2172insA (SNX22)	ENSP00000323435.4:n.*2171_*2172insA
ENST00000557789.5:n.2911_2912insA (SNX22)
ENST00000560997.1:n.2566_2567insA (SNX22)
NM_000942.4:c.528+45_528+46insT , LRG_10t1:c.528+45_528+46insT (PPIB)	NP_000933.1:n.528+45_528+46insT
NM_024798.2:c.*2171_*2172insA (SNX22)	NP_079074.2:n.*2171_*2172insA
NR_073534.1:n.2859_2860insA (SNX22)
XM_017022581.1:c.*2171_*2172insA (SNX22)	XP_016878070.1:n.*2171_*2172insA
NM_024798.3:c.*2171_*2172insA (SNX22) MANE Select	NP_079074.2:n.*2171_*2172insA
NM_000942.5:c.528+45_528+46insT (PPIB) MANE Select	NP_000933.1:n.528+45_528+46insT
NR_073534.2:n.2845_2846insA (SNX22)