Canonical Allele Identifier: CA271410640

Gene: PPIB SNX22

Linked Data

• dbSNP Id: rs542049949
• gnomAD v2: 15-64449319-TGTG-T
• gnomAD v3: 15-64157120-TGTG-T
• gnomAD v4: 15-64157120-TGTG-T
• MyVariant Identifiers: chr15:g.64449320_64449322del (hg19) ; chr15:g.64157121_64157123del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64157124_64157126del , CM000677.2:g.64157124_64157126del	GRCh38
NC_000015.9:g.64449323_64449325del , CM000677.1:g.64449323_64449325del	GRCh37
NC_000015.8:g.62236376_62236378del	NCBI36
NG_012979.1:g.11033_11035del , LRG_10:g.11033_11035del
NG_033071.1:g.10408_10410del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300026.4:c.344-214_344-212del (PPIB) MANE Select	ENSP00000300026.4:n.344-214_344-212del
ENST00000325881.9:c.*2616_*2618del (SNX22) MANE Select	ENSP00000323435.4:n.*2616_*2618del
ENST00000561048.2:n.3357_3359del (PPIB)
ENST00000680158.1:c.*17-214_*17-212del (PPIB)	ENSP00000504873.1:n.*17-214_*17-212del
ENST00000680343.1:n.298-214_298-212del (PPIB)
ENST00000681397.1:c.344-214_344-212del (PPIB)	ENSP00000506584.1:n.344-214_344-212del
ENST00000681658.1:c.239-214_239-212del (PPIB)	ENSP00000505431.1:n.239-214_239-212del
ENST00000300026.3:c.344-214_344-212del (PPIB)	ENSP00000300026.3:n.344-214_344-212del
ENST00000325881.8:c.*2616_*2618del (SNX22)	ENSP00000323435.4:n.*2616_*2618del
ENST00000557789.5:n.3356_3358del (SNX22)
ENST00000558492.1:n.250-214_250-212del (PPIB)
ENST00000560997.1:n.3011_3013del (SNX22)
NM_000942.4:c.344-214_344-212del , LRG_10t1:c.344-214_344-212del (PPIB)	NP_000933.1:n.344-214_344-212del
NM_024798.2:c.*2616_*2618del (SNX22)	NP_079074.2:n.*2616_*2618del
NR_073534.1:n.3304_3306del (SNX22)
XM_017022581.1:c.*2616_*2618del (SNX22)	XP_016878070.1:n.*2616_*2618del
NM_024798.3:c.*2616_*2618del (SNX22) MANE Select	NP_079074.2:n.*2616_*2618del
NM_000942.5:c.344-214_344-212del (PPIB) MANE Select	NP_000933.1:n.344-214_344-212del
NR_073534.2:n.3290_3292del (SNX22)