Canonical Allele Identifier: CA392817398

Gene: PPIB SNX22

Linked Data

• gnomAD v4: 15-64156861-T-C
• MyVariant Identifiers: chr15:g.64449060T>C (hg19) ; chr15:g.64156861T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156861T>C , CM000677.2:g.64156861T>C	GRCh38
NC_000015.9:g.64449060T>C , CM000677.1:g.64449060T>C	GRCh37
NC_000015.8:g.62236113T>C	NCBI36
NG_012979.1:g.11295A>G , LRG_10:g.11295A>G
NG_033071.1:g.10145T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.392A>G (PPIB) MANE Select	ENSP00000300026.4:p.Lys131Arg
ENST00000325881.9:c.*2353T>C (SNX22) MANE Select	ENSP00000323435.4:n.*2353T>C
ENST00000561048.2:n.3619A>G (PPIB)
ENST00000680158.1:c.*65A>G (PPIB)	ENSP00000504873.1:n.*65A>G
ENST00000680343.1:n.346A>G (PPIB)
ENST00000681397.1:c.392A>G (PPIB)	ENSP00000506584.1:p.Lys131Arg
ENST00000681658.1:c.287A>G (PPIB)	ENSP00000505431.1:p.Lys96Arg
ENST00000300026.3:c.392A>G (PPIB)	ENSP00000300026.3:p.Lys131Arg
ENST00000325881.8:c.*2353T>C (SNX22)	ENSP00000323435.4:n.*2353T>C
ENST00000557789.5:n.3093T>C (SNX22)
ENST00000558492.1:n.298A>G (PPIB)
ENST00000560997.1:n.2748T>C (SNX22)
NM_000942.4:c.392A>G , LRG_10t1:c.392A>G (PPIB)	NP_000933.1:p.Lys131Arg
NM_024798.2:c.*2353T>C (SNX22)	NP_079074.2:n.*2353T>C
NR_073534.1:n.3041T>C (SNX22)
XM_017022581.1:c.*2353T>C (SNX22)	XP_016878070.1:n.*2353T>C
NM_024798.3:c.*2353T>C (SNX22) MANE Select	NP_079074.2:n.*2353T>C
NM_000942.5:c.392A>G (PPIB) MANE Select	NP_000933.1:p.Lys131Arg
NR_073534.2:n.3027T>C (SNX22)