Canonical Allele Identifier: CA392816803

Gene: PPIB SNX22

Linked Data

• dbSNP Id: rs1316594476
• gnomAD v2: 15-64448938-C-G
• gnomAD v4: 15-64156739-C-G
• MyVariant Identifiers: chr15:g.64448938C>G (hg19) ; chr15:g.64156739C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156739C>G , CM000677.2:g.64156739C>G	GRCh38
NC_000015.9:g.64448938C>G , CM000677.1:g.64448938C>G	GRCh37
NC_000015.8:g.62235991C>G	NCBI36
NG_012979.1:g.11417G>C , LRG_10:g.11417G>C
NG_033071.1:g.10023C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.514G>C (PPIB) MANE Select	ENSP00000300026.4:p.Val172Leu
ENST00000325881.9:c.*2231C>G (SNX22) MANE Select	ENSP00000323435.4:n.*2231C>G
ENST00000561048.2:n.3741G>C (PPIB)
ENST00000680158.1:c.*187G>C (PPIB)	ENSP00000504873.1:n.*187G>C
ENST00000680343.1:n.468G>C (PPIB)
ENST00000681397.1:c.514G>C (PPIB)	ENSP00000506584.1:p.Val172Leu
ENST00000681658.1:c.409G>C (PPIB)	ENSP00000505431.1:p.Val137Leu
ENST00000300026.3:c.514G>C (PPIB)	ENSP00000300026.3:p.Val172Leu
ENST00000325881.8:c.*2231C>G (SNX22)	ENSP00000323435.4:n.*2231C>G
ENST00000557789.5:n.2971C>G (SNX22)
ENST00000560997.1:n.2626C>G (SNX22)
NM_000942.4:c.514G>C , LRG_10t1:c.514G>C (PPIB)	NP_000933.1:p.Val172Leu
NM_024798.2:c.*2231C>G (SNX22)	NP_079074.2:n.*2231C>G
NR_073534.1:n.2919C>G (SNX22)
XM_017022581.1:c.*2231C>G (SNX22)	XP_016878070.1:n.*2231C>G
NM_024798.3:c.*2231C>G (SNX22) MANE Select	NP_079074.2:n.*2231C>G
NM_000942.5:c.514G>C (PPIB) MANE Select	NP_000933.1:p.Val172Leu
NR_073534.2:n.2905C>G (SNX22)