Canonical Allele Identifier: CA392816774

Gene: PPIB SNX22

Linked Data

• MyVariant Identifiers: chr15:g.64448926T>A (hg19) ; chr15:g.64156727T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156727T>A , CM000677.2:g.64156727T>A	GRCh38
NC_000015.9:g.64448926T>A , CM000677.1:g.64448926T>A	GRCh37
NC_000015.8:g.62235979T>A	NCBI36
NG_012979.1:g.11429A>T , LRG_10:g.11429A>T
NG_033071.1:g.10011T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.526A>T (PPIB) MANE Select	ENSP00000300026.4:p.Met176Leu
ENST00000325881.9:c.*2219T>A (SNX22) MANE Select	ENSP00000323435.4:n.*2219T>A
ENST00000561048.2:n.3753A>T (PPIB)
ENST00000680158.1:c.*199A>T (PPIB)	ENSP00000504873.1:n.*199A>T
ENST00000680343.1:n.480A>T (PPIB)
ENST00000681397.1:c.526A>T (PPIB)	ENSP00000506584.1:p.Met176Leu
ENST00000681658.1:c.421A>T (PPIB)	ENSP00000505431.1:p.Met141Leu
ENST00000300026.3:c.526A>T (PPIB)	ENSP00000300026.3:p.Met176Leu
ENST00000325881.8:c.*2219T>A (SNX22)	ENSP00000323435.4:n.*2219T>A
ENST00000557789.5:n.2959T>A (SNX22)
ENST00000560997.1:n.2614T>A (SNX22)
NM_000942.4:c.526A>T , LRG_10t1:c.526A>T (PPIB)	NP_000933.1:p.Met176Leu
NM_024798.2:c.*2219T>A (SNX22)	NP_079074.2:n.*2219T>A
NR_073534.1:n.2907T>A (SNX22)
XM_017022581.1:c.*2219T>A (SNX22)	XP_016878070.1:n.*2219T>A
NM_024798.3:c.*2219T>A (SNX22) MANE Select	NP_079074.2:n.*2219T>A
NM_000942.5:c.526A>T (PPIB) MANE Select	NP_000933.1:p.Met176Leu
NR_073534.2:n.2893T>A (SNX22)