Canonical Allele Identifier: CA490812152

Gene: PPIB SNX22

Linked Data

• MyVariant Identifiers: chr15:g.64448948C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156749C>A , CM000677.2:g.64156749C>A	GRCh38
NC_000015.9:g.64448948C>A , CM000677.1:g.64448948C>A	GRCh37
NC_000015.8:g.62236001C>A	NCBI36
NG_012979.1:g.11407G>T , LRG_10:g.11407G>T
NG_033071.1:g.10033C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.504G>T (PPIB) MANE Select	ENSP00000300026.4:p.Val168=
ENST00000325881.9:c.*2241C>A (SNX22) MANE Select	ENSP00000323435.4:n.*2241C>A
ENST00000561048.2:n.3731G>T (PPIB)
ENST00000680158.1:c.*177G>T (PPIB)	ENSP00000504873.1:n.*177G>T
ENST00000680343.1:n.458G>T (PPIB)
ENST00000681397.1:c.504G>T (PPIB)	ENSP00000506584.1:p.Val168=
ENST00000681658.1:c.399G>T (PPIB)	ENSP00000505431.1:p.Val133=
ENST00000300026.3:c.504G>T (PPIB)	ENSP00000300026.3:p.Val168=
ENST00000325881.8:c.*2241C>A (SNX22)	ENSP00000323435.4:n.*2241C>A
ENST00000557789.5:n.2981C>A (SNX22)
ENST00000560997.1:n.2636C>A (SNX22)
NM_000942.4:c.504G>T , LRG_10t1:c.504G>T (PPIB)	NP_000933.1:p.Val168=
NM_024798.2:c.*2241C>A (SNX22)	NP_079074.2:n.*2241C>A
NR_073534.1:n.2929C>A (SNX22)
XM_017022581.1:c.*2241C>A (SNX22)	XP_016878070.1:n.*2241C>A
NM_024798.3:c.*2241C>A (SNX22) MANE Select	NP_079074.2:n.*2241C>A
NM_000942.5:c.504G>T (PPIB) MANE Select	NP_000933.1:p.Val168=
NR_073534.2:n.2915C>A (SNX22)