Canonical Allele Identifier: CA2183002583

Gene: PPIB SNX22

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156679C= , CM000677.2:g.64156679C=	GRCh38
NC_000015.9:g.64448878C= , CM000677.1:g.64448878C=	GRCh37
NC_000015.8:g.62235931C=	NCBI36
NG_012979.1:g.11477G= , LRG_10:g.11477G=
NG_033071.1:g.9963C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.528+46G= (PPIB) MANE Select	ENSP00000300026.4:n.528+46G=
ENST00000325881.9:c.*2171C= (SNX22) MANE Select	ENSP00000323435.4:n.*2171C=
ENST00000561048.2:n.3755+46G= (PPIB)
ENST00000680158.1:c.*201+46G= (PPIB)	ENSP00000504873.1:n.*201+46G=
ENST00000680343.1:n.482+46G= (PPIB)
ENST00000681397.1:c.528+46G= (PPIB)	ENSP00000506584.1:n.528+46G=
ENST00000681658.1:c.423+46G= (PPIB)	ENSP00000505431.1:n.423+46G=
ENST00000300026.3:c.528+46G= (PPIB)	ENSP00000300026.3:n.528+46G=
ENST00000325881.8:c.*2171C= (SNX22)	ENSP00000323435.4:n.*2171C=
ENST00000557789.5:n.2911C= (SNX22)
ENST00000560997.1:n.2566C= (SNX22)
NM_000942.4:c.528+46G= , LRG_10t1:c.528+46G= (PPIB)	NP_000933.1:n.528+46G=
NM_024798.2:c.*2171C= (SNX22)	NP_079074.2:n.*2171C=
NR_073534.1:n.2859C= (SNX22)
XM_017022581.1:c.*2171C= (SNX22)	XP_016878070.1:n.*2171C=
NM_024798.3:c.*2171C= (SNX22) MANE Select	NP_079074.2:n.*2171C=
NM_000942.5:c.528+46G= (PPIB) MANE Select	NP_000933.1:n.528+46G=
NR_073534.2:n.2845C= (SNX22)