Canonical Allele Identifier: CA2628930289

Gene: PPIB SNX22

Linked Data

• gnomAD v4: 15-64156704-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156704G>C , CM000677.2:g.64156704G>C	GRCh38
NC_000015.9:g.64448903G>C , CM000677.1:g.64448903G>C	GRCh37
NC_000015.8:g.62235956G>C	NCBI36
NG_012979.1:g.11452C>G , LRG_10:g.11452C>G
NG_033071.1:g.9988G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.528+21C>G (PPIB) MANE Select	ENSP00000300026.4:n.528+21C>G
ENST00000325881.9:c.*2196G>C (SNX22) MANE Select	ENSP00000323435.4:n.*2196G>C
ENST00000561048.2:n.3755+21C>G (PPIB)
ENST00000680158.1:c.*201+21C>G (PPIB)	ENSP00000504873.1:n.*201+21C>G
ENST00000680343.1:n.482+21C>G (PPIB)
ENST00000681397.1:c.528+21C>G (PPIB)	ENSP00000506584.1:n.528+21C>G
ENST00000681658.1:c.423+21C>G (PPIB)	ENSP00000505431.1:n.423+21C>G
ENST00000300026.3:c.528+21C>G (PPIB)	ENSP00000300026.3:n.528+21C>G
ENST00000325881.8:c.*2196G>C (SNX22)	ENSP00000323435.4:n.*2196G>C
ENST00000557789.5:n.2936G>C (SNX22)
ENST00000560997.1:n.2591G>C (SNX22)
NM_000942.4:c.528+21C>G , LRG_10t1:c.528+21C>G (PPIB)	NP_000933.1:n.528+21C>G
NM_024798.2:c.*2196G>C (SNX22)	NP_079074.2:n.*2196G>C
NR_073534.1:n.2884G>C (SNX22)
XM_017022581.1:c.*2196G>C (SNX22)	XP_016878070.1:n.*2196G>C
NM_024798.3:c.*2196G>C (SNX22) MANE Select	NP_079074.2:n.*2196G>C
NM_000942.5:c.528+21C>G (PPIB) MANE Select	NP_000933.1:n.528+21C>G
NR_073534.2:n.2870G>C (SNX22)