Canonical Allele Identifier: CA2183002771

Gene: PPIB SNX22

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64157046G= , CM000677.2:g.64157046G=	GRCh38
NC_000015.9:g.64449245G= , CM000677.1:g.64449245G=	GRCh37
NC_000015.8:g.62236298G=	NCBI36
NG_012979.1:g.11110C= , LRG_10:g.11110C=
NG_033071.1:g.10330G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.344-137C= (PPIB) MANE Select	ENSP00000300026.4:n.344-137C=
ENST00000325881.9:c.*2538G= (SNX22) MANE Select	ENSP00000323435.4:n.*2538G=
ENST00000561048.2:n.3434C= (PPIB)
ENST00000680158.1:c.*17-137C= (PPIB)	ENSP00000504873.1:n.*17-137C=
ENST00000680343.1:n.298-137C= (PPIB)
ENST00000681397.1:c.344-137C= (PPIB)	ENSP00000506584.1:n.344-137C=
ENST00000681658.1:c.239-137C= (PPIB)	ENSP00000505431.1:n.239-137C=
ENST00000300026.3:c.344-137C= (PPIB)	ENSP00000300026.3:n.344-137C=
ENST00000325881.8:c.*2538G= (SNX22)	ENSP00000323435.4:n.*2538G=
ENST00000557789.5:n.3278G= (SNX22)
ENST00000558492.1:n.250-137C= (PPIB)
ENST00000560997.1:n.2933G= (SNX22)
NM_000942.4:c.344-137C= , LRG_10t1:c.344-137C= (PPIB)	NP_000933.1:n.344-137C=
NM_024798.2:c.*2538G= (SNX22)	NP_079074.2:n.*2538G=
NR_073534.1:n.3226G= (SNX22)
XM_017022581.1:c.*2538G= (SNX22)	XP_016878070.1:n.*2538G=
NM_024798.3:c.*2538G= (SNX22) MANE Select	NP_079074.2:n.*2538G=
NM_000942.5:c.344-137C= (PPIB) MANE Select	NP_000933.1:n.344-137C=
NR_073534.2:n.3212G= (SNX22)