Canonical Allele Identifier: CA392816873

Gene: PPIB SNX22

Linked Data

• MyVariant Identifiers: chr15:g.64448953C>A (hg19) ; chr15:g.64156754C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156754C>A , CM000677.2:g.64156754C>A	GRCh38
NC_000015.9:g.64448953C>A , CM000677.1:g.64448953C>A	GRCh37
NC_000015.8:g.62236006C>A	NCBI36
NG_012979.1:g.11402G>T , LRG_10:g.11402G>T
NG_033071.1:g.10038C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.499G>T (PPIB) MANE Select	ENSP00000300026.4:p.Val167Leu
ENST00000325881.9:c.*2246C>A (SNX22) MANE Select	ENSP00000323435.4:n.*2246C>A
ENST00000561048.2:n.3726G>T (PPIB)
ENST00000680158.1:c.*172G>T (PPIB)	ENSP00000504873.1:n.*172G>T
ENST00000680343.1:n.453G>T (PPIB)
ENST00000681397.1:c.499G>T (PPIB)	ENSP00000506584.1:p.Val167Leu
ENST00000681658.1:c.394G>T (PPIB)	ENSP00000505431.1:p.Val132Leu
ENST00000300026.3:c.499G>T (PPIB)	ENSP00000300026.3:p.Val167Leu
ENST00000325881.8:c.*2246C>A (SNX22)	ENSP00000323435.4:n.*2246C>A
ENST00000557789.5:n.2986C>A (SNX22)
ENST00000560997.1:n.2641C>A (SNX22)
NM_000942.4:c.499G>T , LRG_10t1:c.499G>T (PPIB)	NP_000933.1:p.Val167Leu
NM_024798.2:c.*2246C>A (SNX22)	NP_079074.2:n.*2246C>A
NR_073534.1:n.2934C>A (SNX22)
XM_017022581.1:c.*2246C>A (SNX22)	XP_016878070.1:n.*2246C>A
NM_024798.3:c.*2246C>A (SNX22) MANE Select	NP_079074.2:n.*2246C>A
NM_000942.5:c.499G>T (PPIB) MANE Select	NP_000933.1:p.Val167Leu
NR_073534.2:n.2920C>A (SNX22)