Canonical Allele Identifier: CA2183002649

Gene: PPIB SNX22

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156810T= , CM000677.2:g.64156810T=	GRCh38
NC_000015.9:g.64449009T= , CM000677.1:g.64449009T=	GRCh37
NC_000015.8:g.62236062T=	NCBI36
NG_012979.1:g.11346A= , LRG_10:g.11346A=
NG_033071.1:g.10094T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.443A= (PPIB) MANE Select	ENSP00000300026.4:p.Asn148=
ENST00000325881.9:c.*2302T= (SNX22) MANE Select	ENSP00000323435.4:n.*2302T=
ENST00000561048.2:n.3670A= (PPIB)
ENST00000680158.1:c.*116A= (PPIB)	ENSP00000504873.1:n.*116A=
ENST00000680343.1:n.397A= (PPIB)
ENST00000681397.1:c.443A= (PPIB)	ENSP00000506584.1:p.Asn148=
ENST00000681658.1:c.338A= (PPIB)	ENSP00000505431.1:p.Asn113=
ENST00000300026.3:c.443A= (PPIB)	ENSP00000300026.3:p.Asn148=
ENST00000325881.8:c.*2302T= (SNX22)	ENSP00000323435.4:n.*2302T=
ENST00000557789.5:n.3042T= (SNX22)
ENST00000558492.1:n.349A= (PPIB)
ENST00000560997.1:n.2697T= (SNX22)
NM_000942.4:c.443A= , LRG_10t1:c.443A= (PPIB)	NP_000933.1:p.Asn148=
NM_024798.2:c.*2302T= (SNX22)	NP_079074.2:n.*2302T=
NR_073534.1:n.2990T= (SNX22)
XM_017022581.1:c.*2302T= (SNX22)	XP_016878070.1:n.*2302T=
NM_024798.3:c.*2302T= (SNX22) MANE Select	NP_079074.2:n.*2302T=
NM_000942.5:c.443A= (PPIB) MANE Select	NP_000933.1:p.Asn148=
NR_073534.2:n.2976T= (SNX22)