Canonical Allele Identifier: CA490812211

Gene: PPIB SNX22

Linked Data

• MyVariant Identifiers: chr15:g.64449002G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156803G>C , CM000677.2:g.64156803G>C	GRCh38
NC_000015.9:g.64449002G>C , CM000677.1:g.64449002G>C	GRCh37
NC_000015.8:g.62236055G>C	NCBI36
NG_012979.1:g.11353C>G , LRG_10:g.11353C>G
NG_033071.1:g.10087G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.450C>G (PPIB) MANE Select	ENSP00000300026.4:p.Ser150=
ENST00000325881.9:c.*2295G>C (SNX22) MANE Select	ENSP00000323435.4:n.*2295G>C
ENST00000561048.2:n.3677C>G (PPIB)
ENST00000680158.1:c.*123C>G (PPIB)	ENSP00000504873.1:n.*123C>G
ENST00000680343.1:n.404C>G (PPIB)
ENST00000681397.1:c.450C>G (PPIB)	ENSP00000506584.1:p.Ser150=
ENST00000681658.1:c.345C>G (PPIB)	ENSP00000505431.1:p.Ser115=
ENST00000300026.3:c.450C>G (PPIB)	ENSP00000300026.3:p.Ser150=
ENST00000325881.8:c.*2295G>C (SNX22)	ENSP00000323435.4:n.*2295G>C
ENST00000557789.5:n.3035G>C (SNX22)
ENST00000558492.1:n.356C>G (PPIB)
ENST00000560997.1:n.2690G>C (SNX22)
NM_000942.4:c.450C>G , LRG_10t1:c.450C>G (PPIB)	NP_000933.1:p.Ser150=
NM_024798.2:c.*2295G>C (SNX22)	NP_079074.2:n.*2295G>C
NR_073534.1:n.2983G>C (SNX22)
XM_017022581.1:c.*2295G>C (SNX22)	XP_016878070.1:n.*2295G>C
NM_024798.3:c.*2295G>C (SNX22) MANE Select	NP_079074.2:n.*2295G>C
NM_000942.5:c.450C>G (PPIB) MANE Select	NP_000933.1:p.Ser150=
NR_073534.2:n.2969G>C (SNX22)