Canonical Allele Identifier: CA490812230

Gene: PPIB SNX22

Linked Data

• dbSNP Id: rs1596028253
• gnomAD v4: 15-64156824-T-G
• MyVariant Identifiers: chr15:g.64449023T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156824T>G , CM000677.2:g.64156824T>G	GRCh38
NC_000015.9:g.64449023T>G , CM000677.1:g.64449023T>G	GRCh37
NC_000015.8:g.62236076T>G	NCBI36
NG_012979.1:g.11332A>C , LRG_10:g.11332A>C
NG_033071.1:g.10108T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.429A>C (PPIB) MANE Select	ENSP00000300026.4:p.Ala143=
ENST00000325881.9:c.*2316T>G (SNX22) MANE Select	ENSP00000323435.4:n.*2316T>G
ENST00000561048.2:n.3656A>C (PPIB)
ENST00000680158.1:c.*102A>C (PPIB)	ENSP00000504873.1:n.*102A>C
ENST00000680343.1:n.383A>C (PPIB)
ENST00000681397.1:c.429A>C (PPIB)	ENSP00000506584.1:p.Ala143=
ENST00000681658.1:c.324A>C (PPIB)	ENSP00000505431.1:p.Ala108=
ENST00000300026.3:c.429A>C (PPIB)	ENSP00000300026.3:p.Ala143=
ENST00000325881.8:c.*2316T>G (SNX22)	ENSP00000323435.4:n.*2316T>G
ENST00000557789.5:n.3056T>G (SNX22)
ENST00000558492.1:n.335A>C (PPIB)
ENST00000560997.1:n.2711T>G (SNX22)
NM_000942.4:c.429A>C , LRG_10t1:c.429A>C (PPIB)	NP_000933.1:p.Ala143=
NM_024798.2:c.*2316T>G (SNX22)	NP_079074.2:n.*2316T>G
NR_073534.1:n.3004T>G (SNX22)
XM_017022581.1:c.*2316T>G (SNX22)	XP_016878070.1:n.*2316T>G
NM_024798.3:c.*2316T>G (SNX22) MANE Select	NP_079074.2:n.*2316T>G
NM_000942.5:c.429A>C (PPIB) MANE Select	NP_000933.1:p.Ala143=
NR_073534.2:n.2990T>G (SNX22)