Canonical Allele Identifier: CA271410103

Gene: PPIB SNX22

Linked Data

• dbSNP Id: rs879117425
• MyVariant Identifiers: chr15:g.64448918A>C (hg19) ; chr15:g.64156719A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156719A>C , CM000677.2:g.64156719A>C	GRCh38
NC_000015.9:g.64448918A>C , CM000677.1:g.64448918A>C	GRCh37
NC_000015.8:g.62235971A>C	NCBI36
NG_012979.1:g.11437T>G , LRG_10:g.11437T>G
NG_033071.1:g.10003A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.528+6T>G (PPIB) MANE Select	ENSP00000300026.4:n.528+6T>G
ENST00000325881.9:c.*2211A>C (SNX22) MANE Select	ENSP00000323435.4:n.*2211A>C
ENST00000561048.2:n.3755+6T>G (PPIB)
ENST00000680158.1:c.*201+6T>G (PPIB)	ENSP00000504873.1:n.*201+6T>G
ENST00000680343.1:n.482+6T>G (PPIB)
ENST00000681397.1:c.528+6T>G (PPIB)	ENSP00000506584.1:n.528+6T>G
ENST00000681658.1:c.423+6T>G (PPIB)	ENSP00000505431.1:n.423+6T>G
ENST00000300026.3:c.528+6T>G (PPIB)	ENSP00000300026.3:n.528+6T>G
ENST00000325881.8:c.*2211A>C (SNX22)	ENSP00000323435.4:n.*2211A>C
ENST00000557789.5:n.2951A>C (SNX22)
ENST00000560997.1:n.2606A>C (SNX22)
NM_000942.4:c.528+6T>G , LRG_10t1:c.528+6T>G (PPIB)	NP_000933.1:n.528+6T>G
NM_024798.2:c.*2211A>C (SNX22)	NP_079074.2:n.*2211A>C
NR_073534.1:n.2899A>C (SNX22)
XM_017022581.1:c.*2211A>C (SNX22)	XP_016878070.1:n.*2211A>C
NM_024798.3:c.*2211A>C (SNX22) MANE Select	NP_079074.2:n.*2211A>C
NM_000942.5:c.528+6T>G (PPIB) MANE Select	NP_000933.1:n.528+6T>G
NR_073534.2:n.2885A>C (SNX22)