Canonical Allele Identifier: CA490812257

Gene: PPIB SNX22

Linked Data

• MyVariant Identifiers: chr15:g.64449064G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156865G>A , CM000677.2:g.64156865G>A	GRCh38
NC_000015.9:g.64449064G>A , CM000677.1:g.64449064G>A	GRCh37
NC_000015.8:g.62236117G>A	NCBI36
NG_012979.1:g.11291C>T , LRG_10:g.11291C>T
NG_033071.1:g.10149G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.388C>T (PPIB) MANE Select	ENSP00000300026.4:p.Leu130=
ENST00000325881.9:c.*2357G>A (SNX22) MANE Select	ENSP00000323435.4:n.*2357G>A
ENST00000561048.2:n.3615C>T (PPIB)
ENST00000680158.1:c.*61C>T (PPIB)	ENSP00000504873.1:n.*61C>T
ENST00000680343.1:n.342C>T (PPIB)
ENST00000681397.1:c.388C>T (PPIB)	ENSP00000506584.1:p.Leu130=
ENST00000681658.1:c.283C>T (PPIB)	ENSP00000505431.1:p.Leu95=
ENST00000300026.3:c.388C>T (PPIB)	ENSP00000300026.3:p.Leu130=
ENST00000325881.8:c.*2357G>A (SNX22)	ENSP00000323435.4:n.*2357G>A
ENST00000557789.5:n.3097G>A (SNX22)
ENST00000558492.1:n.294C>T (PPIB)
ENST00000560997.1:n.2752G>A (SNX22)
NM_000942.4:c.388C>T , LRG_10t1:c.388C>T (PPIB)	NP_000933.1:p.Leu130=
NM_024798.2:c.*2357G>A (SNX22)	NP_079074.2:n.*2357G>A
NR_073534.1:n.3045G>A (SNX22)
XM_017022581.1:c.*2357G>A (SNX22)	XP_016878070.1:n.*2357G>A
NM_024798.3:c.*2357G>A (SNX22) MANE Select	NP_079074.2:n.*2357G>A
NM_000942.5:c.388C>T (PPIB) MANE Select	NP_000933.1:p.Leu130=
NR_073534.2:n.3031G>A (SNX22)