Canonical Allele Identifier: CA2183002611

Gene: PPIB SNX22

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156734T= , CM000677.2:g.64156734T=	GRCh38
NC_000015.9:g.64448933T= , CM000677.1:g.64448933T=	GRCh37
NC_000015.8:g.62235986T=	NCBI36
NG_012979.1:g.11422A= , LRG_10:g.11422A=
NG_033071.1:g.10018T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.519A= (PPIB) MANE Select	ENSP00000300026.4:p.Leu173=
ENST00000325881.9:c.*2226T= (SNX22) MANE Select	ENSP00000323435.4:n.*2226T=
ENST00000561048.2:n.3746A= (PPIB)
ENST00000680158.1:c.*192A= (PPIB)	ENSP00000504873.1:n.*192A=
ENST00000680343.1:n.473A= (PPIB)
ENST00000681397.1:c.519A= (PPIB)	ENSP00000506584.1:p.Leu173=
ENST00000681658.1:c.414A= (PPIB)	ENSP00000505431.1:p.Leu138=
ENST00000300026.3:c.519A= (PPIB)	ENSP00000300026.3:p.Leu173=
ENST00000325881.8:c.*2226T= (SNX22)	ENSP00000323435.4:n.*2226T=
ENST00000557789.5:n.2966T= (SNX22)
ENST00000560997.1:n.2621T= (SNX22)
NM_000942.4:c.519A= , LRG_10t1:c.519A= (PPIB)	NP_000933.1:p.Leu173=
NM_024798.2:c.*2226T= (SNX22)	NP_079074.2:n.*2226T=
NR_073534.1:n.2914T= (SNX22)
XM_017022581.1:c.*2226T= (SNX22)	XP_016878070.1:n.*2226T=
NM_024798.3:c.*2226T= (SNX22) MANE Select	NP_079074.2:n.*2226T=
NM_000942.5:c.519A= (PPIB) MANE Select	NP_000933.1:p.Leu173=
NR_073534.2:n.2900T= (SNX22)