Canonical Allele Identifier: CA2628930563

Gene: PPIB SNX22

Linked Data

• gnomAD v4: 15-64156862-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156863del , CM000677.2:g.64156863del	GRCh38
NC_000015.9:g.64449062del , CM000677.1:g.64449062del	GRCh37
NC_000015.8:g.62236115del	NCBI36
NG_012979.1:g.11293del , LRG_10:g.11293del
NG_033071.1:g.10147del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.390del (PPIB) MANE Select	ENSP00000300026.4:p.Lys131SerfsTer8
ENST00000325881.9:c.*2355del (SNX22) MANE Select	ENSP00000323435.4:n.*2355del
ENST00000561048.2:n.3617del (PPIB)
ENST00000680158.1:c.*63del (PPIB)	ENSP00000504873.1:n.*63del
ENST00000680343.1:n.344del (PPIB)
ENST00000681397.1:c.390del (PPIB)	ENSP00000506584.1:p.Lys131SerfsTer8
ENST00000681658.1:c.285del (PPIB)	ENSP00000505431.1:p.Lys96SerfsTer8
ENST00000300026.3:c.390del (PPIB)	ENSP00000300026.3:p.Lys131SerfsTer8
ENST00000325881.8:c.*2355del (SNX22)	ENSP00000323435.4:n.*2355del
ENST00000557789.5:n.3095del (SNX22)
ENST00000558492.1:n.296del (PPIB)
ENST00000560997.1:n.2750del (SNX22)
NM_000942.4:c.390del , LRG_10t1:c.390del (PPIB)	NP_000933.1:p.Lys131SerfsTer8
NM_024798.2:c.*2355del (SNX22)	NP_079074.2:n.*2355del
NR_073534.1:n.3043del (SNX22)
XM_017022581.1:c.*2355del (SNX22)	XP_016878070.1:n.*2355del
NM_024798.3:c.*2355del (SNX22) MANE Select	NP_079074.2:n.*2355del
NM_000942.5:c.390del (PPIB) MANE Select	NP_000933.1:p.Lys131SerfsTer8
NR_073534.2:n.3029del (SNX22)