Canonical Allele Identifier: CA2628931039

Gene: PPIB SNX22

Linked Data

• gnomAD v4: 15-64157054-C-CCTAT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64157057_64157060dup , CM000677.2:g.64157057_64157060dup	GRCh38
NC_000015.9:g.64449256_64449259dup , CM000677.1:g.64449256_64449259dup	GRCh37
NC_000015.8:g.62236309_62236312dup	NCBI36
NG_012979.1:g.11098_11101dup , LRG_10:g.11098_11101dup
NG_033071.1:g.10341_10344dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.344-149_344-146dup (PPIB) MANE Select	ENSP00000300026.4:n.344-149_344-146dup
ENST00000325881.9:c.*2549_*2552dup (SNX22) MANE Select	ENSP00000323435.4:n.*2549_*2552dup
ENST00000561048.2:n.3422_3425dup (PPIB)
ENST00000680158.1:c.*17-149_*17-146dup (PPIB)	ENSP00000504873.1:n.*17-149_*17-146dup
ENST00000680343.1:n.298-149_298-146dup (PPIB)
ENST00000681397.1:c.344-149_344-146dup (PPIB)	ENSP00000506584.1:n.344-149_344-146dup
ENST00000681658.1:c.239-149_239-146dup (PPIB)	ENSP00000505431.1:n.239-149_239-146dup
ENST00000300026.3:c.344-149_344-146dup (PPIB)	ENSP00000300026.3:n.344-149_344-146dup
ENST00000325881.8:c.*2549_*2552dup (SNX22)	ENSP00000323435.4:n.*2549_*2552dup
ENST00000557789.5:n.3289_3292dup (SNX22)
ENST00000558492.1:n.250-149_250-146dup (PPIB)
ENST00000560997.1:n.2944_2947dup (SNX22)
NM_000942.4:c.344-149_344-146dup , LRG_10t1:c.344-149_344-146dup (PPIB)	NP_000933.1:n.344-149_344-146dup
NM_024798.2:c.*2549_*2552dup (SNX22)	NP_079074.2:n.*2549_*2552dup
NR_073534.1:n.3237_3240dup (SNX22)
XM_017022581.1:c.*2549_*2552dup (SNX22)	XP_016878070.1:n.*2549_*2552dup
NM_024798.3:c.*2549_*2552dup (SNX22) MANE Select	NP_079074.2:n.*2549_*2552dup
NM_000942.5:c.344-149_344-146dup (PPIB) MANE Select	NP_000933.1:n.344-149_344-146dup
NR_073534.2:n.3223_3226dup (SNX22)