Canonical Allele Identifier: CA392817104

Gene: PPIB SNX22

Linked Data

• MyVariant Identifiers: chr15:g.64449001G>T (hg19) ; chr15:g.64156802G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156802G>T , CM000677.2:g.64156802G>T	GRCh38
NC_000015.9:g.64449001G>T , CM000677.1:g.64449001G>T	GRCh37
NC_000015.8:g.62236054G>T	NCBI36
NG_012979.1:g.11354C>A , LRG_10:g.11354C>A
NG_033071.1:g.10086G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.451C>A (PPIB) MANE Select	ENSP00000300026.4:p.Gln151Lys
ENST00000325881.9:c.*2294G>T (SNX22) MANE Select	ENSP00000323435.4:n.*2294G>T
ENST00000561048.2:n.3678C>A (PPIB)
ENST00000680158.1:c.*124C>A (PPIB)	ENSP00000504873.1:n.*124C>A
ENST00000680343.1:n.405C>A (PPIB)
ENST00000681397.1:c.451C>A (PPIB)	ENSP00000506584.1:p.Gln151Lys
ENST00000681658.1:c.346C>A (PPIB)	ENSP00000505431.1:p.Gln116Lys
ENST00000300026.3:c.451C>A (PPIB)	ENSP00000300026.3:p.Gln151Lys
ENST00000325881.8:c.*2294G>T (SNX22)	ENSP00000323435.4:n.*2294G>T
ENST00000557789.5:n.3034G>T (SNX22)
ENST00000558492.1:n.357C>A (PPIB)
ENST00000560997.1:n.2689G>T (SNX22)
NM_000942.4:c.451C>A , LRG_10t1:c.451C>A (PPIB)	NP_000933.1:p.Gln151Lys
NM_024798.2:c.*2294G>T (SNX22)	NP_079074.2:n.*2294G>T
NR_073534.1:n.2982G>T (SNX22)
XM_017022581.1:c.*2294G>T (SNX22)	XP_016878070.1:n.*2294G>T
NM_024798.3:c.*2294G>T (SNX22) MANE Select	NP_079074.2:n.*2294G>T
NM_000942.5:c.451C>A (PPIB) MANE Select	NP_000933.1:p.Gln151Lys
NR_073534.2:n.2968G>T (SNX22)