Canonical Allele Identifier: CA618610012

Gene: PPIB SNX22

Linked Data

• dbSNP Id: rs1268399080
• gnomAD v2: 15-64449340-G-T
• gnomAD v3: 15-64157141-G-T
• gnomAD v4: 15-64157141-G-T
• MyVariant Identifiers: chr15:g.64449340G>T (hg19) ; chr15:g.64157141G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64157141G>T , CM000677.2:g.64157141G>T	GRCh38
NC_000015.9:g.64449340G>T , CM000677.1:g.64449340G>T	GRCh37
NC_000015.8:g.62236393G>T	NCBI36
NG_012979.1:g.11015C>A , LRG_10:g.11015C>A
NG_033071.1:g.10425G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.344-232C>A (PPIB) MANE Select	ENSP00000300026.4:n.344-232C>A
ENST00000325881.9:c.*2633G>T (SNX22) MANE Select	ENSP00000323435.4:n.*2633G>T
ENST00000561048.2:n.3339C>A (PPIB)
ENST00000680158.1:c.*17-232C>A (PPIB)	ENSP00000504873.1:n.*17-232C>A
ENST00000680343.1:n.298-232C>A (PPIB)
ENST00000681397.1:c.344-232C>A (PPIB)	ENSP00000506584.1:n.344-232C>A
ENST00000681658.1:c.239-232C>A (PPIB)	ENSP00000505431.1:n.239-232C>A
ENST00000300026.3:c.344-232C>A (PPIB)	ENSP00000300026.3:n.344-232C>A
ENST00000325881.8:c.*2633G>T (SNX22)	ENSP00000323435.4:n.*2633G>T
ENST00000557789.5:n.3373G>T (SNX22)
ENST00000558492.1:n.250-232C>A (PPIB)
ENST00000560997.1:n.3028G>T (SNX22)
NM_000942.4:c.344-232C>A , LRG_10t1:c.344-232C>A (PPIB)	NP_000933.1:n.344-232C>A
NM_024798.2:c.*2633G>T (SNX22)	NP_079074.2:n.*2633G>T
NR_073534.1:n.3321G>T (SNX22)
XM_017022581.1:c.*2633G>T (SNX22)	XP_016878070.1:n.*2633G>T
NM_024798.3:c.*2633G>T (SNX22) MANE Select	NP_079074.2:n.*2633G>T
NM_000942.5:c.344-232C>A (PPIB) MANE Select	NP_000933.1:n.344-232C>A
NR_073534.2:n.3307G>T (SNX22)