Canonical Allele Identifier: CA2628931143

Gene: PPIB SNX22

Linked Data

• gnomAD v4: 15-64157091-A-ATGCCCCACTT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64157091_64157092insTGCCCCACTT , CM000677.2:g.64157091_64157092insTGCCCCACTT	GRCh38
NC_000015.9:g.64449290_64449291insTGCCCCACTT , CM000677.1:g.64449290_64449291insTGCCCCACTT	GRCh37
NC_000015.8:g.62236343_62236344insTGCCCCACTT	NCBI36
NG_012979.1:g.11064_11065insAAGTGGGGCA , LRG_10:g.11064_11065insAAGTGGGGCA
NG_033071.1:g.10375_10376insTGCCCCACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.344-183_344-182insAAGTGGGGCA (PPIB) MANE Select	ENSP00000300026.4:n.344-183_344-182insAAGTGGGGCA
ENST00000325881.9:c.*2583_*2584insTGCCCCACTT (SNX22) MANE Select	ENSP00000323435.4:n.*2583_*2584insTGCCCCACTT
ENST00000561048.2:n.3388_3389insAAGTGGGGCA (PPIB)
ENST00000680158.1:c.*17-183_*17-182insAAGTGGGGCA (PPIB)	ENSP00000504873.1:n.*17-183_*17-182insAAGTGGGGCA
ENST00000680343.1:n.298-183_298-182insAAGTGGGGCA (PPIB)
ENST00000681397.1:c.344-183_344-182insAAGTGGGGCA (PPIB)	ENSP00000506584.1:n.344-183_344-182insAAGTGGGGCA
ENST00000681658.1:c.239-183_239-182insAAGTGGGGCA (PPIB)	ENSP00000505431.1:n.239-183_239-182insAAGTGGGGCA
ENST00000300026.3:c.344-183_344-182insAAGTGGGGCA (PPIB)	ENSP00000300026.3:n.344-183_344-182insAAGTGGGGCA
ENST00000325881.8:c.*2583_*2584insTGCCCCACTT (SNX22)	ENSP00000323435.4:n.*2583_*2584insTGCCCCACTT
ENST00000557789.5:n.3323_3324insTGCCCCACTT (SNX22)
ENST00000558492.1:n.250-183_250-182insAAGTGGGGCA (PPIB)
ENST00000560997.1:n.2978_2979insTGCCCCACTT (SNX22)
NM_000942.4:c.344-183_344-182insAAGTGGGGCA , LRG_10t1:c.344-183_344-182insAAGTGGGGCA (PPIB)	NP_000933.1:n.344-183_344-182insAAGTGGGGCA
NM_024798.2:c.*2583_*2584insTGCCCCACTT (SNX22)	NP_079074.2:n.*2583_*2584insTGCCCCACTT
NR_073534.1:n.3271_3272insTGCCCCACTT (SNX22)
XM_017022581.1:c.*2583_*2584insTGCCCCACTT (SNX22)	XP_016878070.1:n.*2583_*2584insTGCCCCACTT
NM_024798.3:c.*2583_*2584insTGCCCCACTT (SNX22) MANE Select	NP_079074.2:n.*2583_*2584insTGCCCCACTT
NM_000942.5:c.344-183_344-182insAAGTGGGGCA (PPIB) MANE Select	NP_000933.1:n.344-183_344-182insAAGTGGGGCA
NR_073534.2:n.3257_3258insTGCCCCACTT (SNX22)