Canonical Allele Identifier: CA392817113

Gene: PPIB SNX22

Linked Data

• MyVariant Identifiers: chr15:g.64449003G>T (hg19) ; chr15:g.64156804G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156804G>T , CM000677.2:g.64156804G>T	GRCh38
NC_000015.9:g.64449003G>T , CM000677.1:g.64449003G>T	GRCh37
NC_000015.8:g.62236056G>T	NCBI36
NG_012979.1:g.11352C>A , LRG_10:g.11352C>A
NG_033071.1:g.10088G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.449C>A (PPIB) MANE Select	ENSP00000300026.4:p.Ser150Tyr
ENST00000325881.9:c.*2296G>T (SNX22) MANE Select	ENSP00000323435.4:n.*2296G>T
ENST00000561048.2:n.3676C>A (PPIB)
ENST00000680158.1:c.*122C>A (PPIB)	ENSP00000504873.1:n.*122C>A
ENST00000680343.1:n.403C>A (PPIB)
ENST00000681397.1:c.449C>A (PPIB)	ENSP00000506584.1:p.Ser150Tyr
ENST00000681658.1:c.344C>A (PPIB)	ENSP00000505431.1:p.Ser115Tyr
ENST00000300026.3:c.449C>A (PPIB)	ENSP00000300026.3:p.Ser150Tyr
ENST00000325881.8:c.*2296G>T (SNX22)	ENSP00000323435.4:n.*2296G>T
ENST00000557789.5:n.3036G>T (SNX22)
ENST00000558492.1:n.355C>A (PPIB)
ENST00000560997.1:n.2691G>T (SNX22)
NM_000942.4:c.449C>A , LRG_10t1:c.449C>A (PPIB)	NP_000933.1:p.Ser150Tyr
NM_024798.2:c.*2296G>T (SNX22)	NP_079074.2:n.*2296G>T
NR_073534.1:n.2984G>T (SNX22)
XM_017022581.1:c.*2296G>T (SNX22)	XP_016878070.1:n.*2296G>T
NM_024798.3:c.*2296G>T (SNX22) MANE Select	NP_079074.2:n.*2296G>T
NM_000942.5:c.449C>A (PPIB) MANE Select	NP_000933.1:p.Ser150Tyr
NR_073534.2:n.2970G>T (SNX22)