Canonical Allele Identifier: CA2575755591

Gene: PPIB SNX22

Linked Data

• gnomAD v4: 15-64157006-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64157008del , CM000677.2:g.64157008del	GRCh38
NC_000015.9:g.64449207del , CM000677.1:g.64449207del	GRCh37
NC_000015.8:g.62236260del	NCBI36
NG_012979.1:g.11149del , LRG_10:g.11149del
NG_033071.1:g.10292del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.344-98del (PPIB) MANE Select	ENSP00000300026.4:n.344-98del
ENST00000325881.9:c.*2500del (SNX22) MANE Select	ENSP00000323435.4:n.*2500del
ENST00000561048.2:n.3473del (PPIB)
ENST00000680158.1:c.*17-98del (PPIB)	ENSP00000504873.1:n.*17-98del
ENST00000680343.1:n.298-98del (PPIB)
ENST00000681397.1:c.344-98del (PPIB)	ENSP00000506584.1:n.344-98del
ENST00000681658.1:c.239-98del (PPIB)	ENSP00000505431.1:n.239-98del
ENST00000300026.3:c.344-98del (PPIB)	ENSP00000300026.3:n.344-98del
ENST00000325881.8:c.*2500del (SNX22)	ENSP00000323435.4:n.*2500del
ENST00000557789.5:n.3240del (SNX22)
ENST00000558492.1:n.250-98del (PPIB)
ENST00000560997.1:n.2895del (SNX22)
NM_000942.4:c.344-98del , LRG_10t1:c.344-98del (PPIB)	NP_000933.1:n.344-98del
NM_024798.2:c.*2500del (SNX22)	NP_079074.2:n.*2500del
NR_073534.1:n.3188del (SNX22)
XM_017022581.1:c.*2500del (SNX22)	XP_016878070.1:n.*2500del
NM_024798.3:c.*2500del (SNX22) MANE Select	NP_079074.2:n.*2500del
NM_000942.5:c.344-98del (PPIB) MANE Select	NP_000933.1:n.344-98del
NR_073534.2:n.3174del (SNX22)