Canonical Allele Identifier: CA3360799

Gene: PPIP5K2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.103201656T>C , CM000667.2:g.103201656T>C	GRCh38
NC_000005.9:g.102537357T>C , CM000667.1:g.102537357T>C	GRCh37
NC_000005.8:g.102565256T>C	NCBI36
NG_051568.1:g.86409T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001276277.3:c.*22T>C MANE Select	NP_001263206.1:n.*22T>C
ENST00000358359.8:c.*22T>C MANE Select	ENSP00000351126.3:n.*22T>C
NM_001276277.1:c.*22T>C	NP_001263206.1:n.*22T>C
NM_001276277.2:c.*22T>C	NP_001263206.1:n.*22T>C
NM_001281471.1:c.*22T>C	NP_001268400.1:n.*22T>C
NM_001281471.2:c.*22T>C	NP_001268400.1:n.*22T>C
NM_001281471.3:c.*22T>C	NP_001268400.1:n.*22T>C
NM_001345871.1:c.*22T>C	NP_001332800.1:n.*22T>C
NM_001345871.2:c.*22T>C	NP_001332800.1:n.*22T>C
NM_001345872.1:c.*22T>C	NP_001332801.1:n.*22T>C
NM_001345872.2:c.*22T>C	NP_001332801.1:n.*22T>C
NM_001345873.1:c.*22T>C	NP_001332802.1:n.*22T>C
NM_001345873.2:c.*22T>C	NP_001332802.1:n.*22T>C
NM_001345874.1:c.*22T>C	NP_001332803.1:n.*22T>C
NM_001345874.2:c.*22T>C	NP_001332803.1:n.*22T>C
NM_001345875.1:c.*22T>C	NP_001332804.1:n.*22T>C
NM_001345875.2:c.*22T>C	NP_001332804.1:n.*22T>C
NM_001345876.1:c.*22T>C	NP_001332805.1:n.*22T>C
NM_001345876.2:c.*22T>C	NP_001332805.1:n.*22T>C
NM_001345877.1:c.*22T>C	NP_001332806.1:n.*22T>C
NM_001345877.2:c.*22T>C	NP_001332806.1:n.*22T>C
NM_001345878.1:c.*22T>C	NP_001332807.1:n.*22T>C
NM_001345878.2:c.*22T>C	NP_001332807.1:n.*22T>C
NM_015216.3:c.*22T>C	NP_056031.2:n.*22T>C
NM_015216.4:c.*22T>C	NP_056031.2:n.*22T>C
NM_015216.5:c.*22T>C	NP_056031.2:n.*22T>C
ENST00000321521.13:c.*22T>C	ENSP00000313070.8:n.*22T>C
ENST00000358359.7:c.*22T>C	ENSP00000351126.3:n.*22T>C
ENST00000414217.5:c.*22T>C	ENSP00000416016.1:n.*22T>C
ENST00000504083.1:n.380T>C
ENST00000509597.5:c.1219T>C	ENSP00000424948.1:n.1219T>C
ENST00000613674.4:c.*22T>C	ENSP00000482907.1:n.*22T>C
ENST00000627916.2:c.*22T>C	ENSP00000486357.1:n.*22T>C
ENST00000698750.1:c.*22T>C	ENSP00000513912.1:n.*22T>C
XM_005271935.1:c.*22T>C	XP_005271992.1:n.*22T>C
XM_005271936.1:c.*22T>C	XP_005271993.1:n.*22T>C
XM_005271938.1:c.*22T>C	XP_005271995.1:n.*22T>C
XM_005277534.1:c.*22T>C	XP_005277591.1:n.*22T>C
XM_005277534.2:c.*22T>C	XP_005277591.1:n.*22T>C
XM_005277535.1:c.*22T>C	XP_005277592.1:n.*22T>C
XM_005277535.2:c.*22T>C	XP_005277592.1:n.*22T>C
XM_005277536.1:c.*22T>C	XP_005277593.1:n.*22T>C
XM_005277536.2:c.*22T>C	XP_005277593.1:n.*22T>C
XM_005277538.1:c.*22T>C	XP_005277595.1:n.*22T>C
XM_005277539.1:c.*22T>C	XP_005277596.1:n.*22T>C
XM_005277539.2:c.*22T>C	XP_005277596.1:n.*22T>C
XM_005277541.1:c.*22T>C	XP_005277598.1:n.*22T>C
XM_005277541.2:c.*22T>C	XP_005277598.1:n.*22T>C
XM_006714576.1:c.*22T>C	XP_006714639.1:n.*22T>C
XM_006714576.2:c.*22T>C	XP_006714639.1:n.*22T>C
XM_006714577.1:c.*22T>C	XP_006714640.1:n.*22T>C
XM_006714577.2:c.*22T>C	XP_006714640.1:n.*22T>C
XM_017009273.2:c.*22T>C	XP_016864762.1:n.*22T>C
XM_017009274.2:c.*22T>C	XP_016864763.1:n.*22T>C