Canonical Allele Identifier: CA392817402

Gene: PPIB SNX22

Linked Data

• MyVariant Identifiers: chr15:g.64449061T>C (hg19) ; chr15:g.64156862T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.64156862T>C , CM000677.2:g.64156862T>C	GRCh38
NC_000015.9:g.64449061T>C , CM000677.1:g.64449061T>C	GRCh37
NC_000015.8:g.62236114T>C	NCBI36
NG_012979.1:g.11294A>G , LRG_10:g.11294A>G
NG_033071.1:g.10146T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000300026.4:c.391A>G (PPIB) MANE Select	ENSP00000300026.4:p.Lys131Glu
ENST00000325881.9:c.*2354T>C (SNX22) MANE Select	ENSP00000323435.4:n.*2354T>C
ENST00000561048.2:n.3618A>G (PPIB)
ENST00000680158.1:c.*64A>G (PPIB)	ENSP00000504873.1:n.*64A>G
ENST00000680343.1:n.345A>G (PPIB)
ENST00000681397.1:c.391A>G (PPIB)	ENSP00000506584.1:p.Lys131Glu
ENST00000681658.1:c.286A>G (PPIB)	ENSP00000505431.1:p.Lys96Glu
ENST00000300026.3:c.391A>G (PPIB)	ENSP00000300026.3:p.Lys131Glu
ENST00000325881.8:c.*2354T>C (SNX22)	ENSP00000323435.4:n.*2354T>C
ENST00000557789.5:n.3094T>C (SNX22)
ENST00000558492.1:n.297A>G (PPIB)
ENST00000560997.1:n.2749T>C (SNX22)
NM_000942.4:c.391A>G , LRG_10t1:c.391A>G (PPIB)	NP_000933.1:p.Lys131Glu
NM_024798.2:c.*2354T>C (SNX22)	NP_079074.2:n.*2354T>C
NR_073534.1:n.3042T>C (SNX22)
XM_017022581.1:c.*2354T>C (SNX22)	XP_016878070.1:n.*2354T>C
NM_024798.3:c.*2354T>C (SNX22) MANE Select	NP_079074.2:n.*2354T>C
NM_000942.5:c.391A>G (PPIB) MANE Select	NP_000933.1:p.Lys131Glu
NR_073534.2:n.3028T>C (SNX22)