Canonical Allele Identifier: CA392816834

Gene: PPIB SNX22

Linked Data

• MyVariant Identifiers: chr15:g.64448944C>T (hg19) ; chr15:g.64156745C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156745C>T , CM000677.2:g.64156745C>T	GRCh38
NC_000015.9:g.64448944C>T , CM000677.1:g.64448944C>T	GRCh37
NC_000015.8:g.62235997C>T	NCBI36
NG_012979.1:g.11411G>A , LRG_10:g.11411G>A
NG_033071.1:g.10029C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.508G>A (PPIB) MANE Select	ENSP00000300026.4:p.Gly170Ser
ENST00000325881.9:c.*2237C>T (SNX22) MANE Select	ENSP00000323435.4:n.*2237C>T
ENST00000561048.2:n.3735G>A (PPIB)
ENST00000680158.1:c.*181G>A (PPIB)	ENSP00000504873.1:n.*181G>A
ENST00000680343.1:n.462G>A (PPIB)
ENST00000681397.1:c.508G>A (PPIB)	ENSP00000506584.1:p.Gly170Ser
ENST00000681658.1:c.403G>A (PPIB)	ENSP00000505431.1:p.Gly135Ser
ENST00000300026.3:c.508G>A (PPIB)	ENSP00000300026.3:p.Gly170Ser
ENST00000325881.8:c.*2237C>T (SNX22)	ENSP00000323435.4:n.*2237C>T
ENST00000557789.5:n.2977C>T (SNX22)
ENST00000560997.1:n.2632C>T (SNX22)
NM_000942.4:c.508G>A , LRG_10t1:c.508G>A (PPIB)	NP_000933.1:p.Gly170Ser
NM_024798.2:c.*2237C>T (SNX22)	NP_079074.2:n.*2237C>T
NR_073534.1:n.2925C>T (SNX22)
XM_017022581.1:c.*2237C>T (SNX22)	XP_016878070.1:n.*2237C>T
NM_024798.3:c.*2237C>T (SNX22) MANE Select	NP_079074.2:n.*2237C>T
NM_000942.5:c.508G>A (PPIB) MANE Select	NP_000933.1:p.Gly170Ser
NR_073534.2:n.2911C>T (SNX22)