Canonical Allele Identifier: CA397535583
Gene: INPP5K HGNC NCBI

Linked Data

gnomAD v4: 17-1495853-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1495853G>T , CM000679.2:g.1495853G>T GRCh38
NC_000017.10:g.1399147G>T , CM000679.1:g.1399147G>T GRCh37
NC_000017.9:g.1345897G>T NCBI36
NG_029891.1:g.26036C>A
NG_047063.1:g.1855C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000421807.7:c.1317C>A MANE Select ENSP00000413937.2:p.Asp439Glu
ENST00000320345.10:c.1089C>A ENSP00000318476.6:p.Asp363Glu
ENST00000350761.9:c.*908C>A ENSP00000254712.5:n.*908C>A
ENST00000406424.8:c.1089C>A ENSP00000385177.4:p.Asp363Glu
ENST00000421807.6:c.1317C>A ENSP00000413937.2:p.Asp439Glu
ENST00000487039.1:n.429C>A
NM_001135642.1:c.1089C>A NP_001129114.1:p.Asp363Glu
NM_016532.3:c.1317C>A NP_057616.2:p.Asp439Glu
NM_130766.2:c.1089C>A NP_570122.1:p.Asp363Glu
XM_005256683.2:c.1089C>A XP_005256740.1:p.Asp363Glu
XM_005256685.1:c.1041C>A XP_005256742.1:p.Asp347Glu
XM_005256686.1:c.1041C>A XP_005256743.1:p.Asp347Glu
XM_011523934.1:c.1089C>A XP_011522236.1:p.Asp363Glu
XM_011523935.1:c.1089C>A XP_011522237.1:p.Asp363Glu
XM_011523936.1:c.912C>A XP_011522238.1:p.Asp304Glu
XM_005256686.2:c.1041C>A XP_005256743.1:p.Asp347Glu
XM_011523936.2:c.912C>A XP_011522238.1:p.Asp304Glu
XM_017024756.1:c.1089C>A XP_016880245.1:p.Asp363Glu
XM_017024757.2:c.1041C>A XP_016880246.1:p.Asp347Glu
XM_017024758.2:c.912C>A XP_016880247.1:p.Asp304Glu
XM_017024759.1:c.912C>A XP_016880248.1:p.Asp304Glu
XM_024450802.1:c.1089C>A XP_024306570.1:p.Asp363Glu
NM_016532.4:c.1317C>A MANE Select NP_057616.2:p.Asp439Glu
NM_001135642.2:c.1089C>A NP_001129114.1:p.Asp363Glu
NM_130766.3:c.1089C>A NP_570122.1:p.Asp363Glu