Canonical Allele Identifier: CA7608501

Gene: PPIB SNX22

Linked Data

• dbSNP Id: rs374880244
• ExAC: 15:64449125 A / T
• gnomAD v2: 15-64449125-A-T
• MyVariant Identifiers: chr15:g.64449125A>T (hg19) ; chr15:g.64156926A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156926A>T , CM000677.2:g.64156926A>T	GRCh38
NC_000015.9:g.64449125A>T , CM000677.1:g.64449125A>T	GRCh37
NC_000015.8:g.62236178A>T	NCBI36
NG_012979.1:g.11230T>A , LRG_10:g.11230T>A
NG_033071.1:g.10210A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.344-17T>A (PPIB) MANE Select	ENSP00000300026.4:n.344-17T>A
ENST00000325881.9:c.*2418A>T (SNX22) MANE Select	ENSP00000323435.4:n.*2418A>T
ENST00000561048.2:n.3554T>A (PPIB)
ENST00000680158.1:c.*17-17T>A (PPIB)	ENSP00000504873.1:n.*17-17T>A
ENST00000680343.1:n.298-17T>A (PPIB)
ENST00000681397.1:c.344-17T>A (PPIB)	ENSP00000506584.1:n.344-17T>A
ENST00000681658.1:c.239-17T>A (PPIB)	ENSP00000505431.1:n.239-17T>A
ENST00000300026.3:c.344-17T>A (PPIB)	ENSP00000300026.3:n.344-17T>A
ENST00000325881.8:c.*2418A>T (SNX22)	ENSP00000323435.4:n.*2418A>T
ENST00000557789.5:n.3158A>T (SNX22)
ENST00000558492.1:n.250-17T>A (PPIB)
ENST00000560997.1:n.2813A>T (SNX22)
NM_000942.4:c.344-17T>A , LRG_10t1:c.344-17T>A (PPIB)	NP_000933.1:n.344-17T>A
NM_024798.2:c.*2418A>T (SNX22)	NP_079074.2:n.*2418A>T
NR_073534.1:n.3106A>T (SNX22)
XM_017022581.1:c.*2418A>T (SNX22)	XP_016878070.1:n.*2418A>T
NM_024798.3:c.*2418A>T (SNX22) MANE Select	NP_079074.2:n.*2418A>T
NM_000942.5:c.344-17T>A (PPIB) MANE Select	NP_000933.1:n.344-17T>A
NR_073534.2:n.3092A>T (SNX22)