Canonical Allele Identifier: CA2242889373
Gene: INPP5K HGNC NCBI

Linked Data

dbSNP Id: rs2074833398

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1496240A>T , CM000679.2:g.1496240A>T GRCh38
NC_000017.10:g.1399534A>T , CM000679.1:g.1399534A>T GRCh37
NC_000017.9:g.1346284A>T NCBI36
NG_029891.1:g.25649T>A
NG_047063.1:g.1468T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000421807.7:c.1186-76T>A MANE Select ENSP00000413937.2:n.1186-76T>A
ENST00000320345.10:c.958-76T>A ENSP00000318476.6:n.958-76T>A
ENST00000350761.9:c.*777-76T>A ENSP00000254712.5:n.*777-76T>A
ENST00000406424.8:c.958-76T>A ENSP00000385177.4:n.958-76T>A
ENST00000421807.6:c.1186-76T>A ENSP00000413937.2:n.1186-76T>A
ENST00000487039.1:n.222T>A
ENST00000574561.1:c.454-76T>A ENSP00000461105.1:n.454-76T>A
NM_001135642.1:c.958-76T>A NP_001129114.1:n.958-76T>A
NM_016532.3:c.1186-76T>A NP_057616.2:n.1186-76T>A
NM_130766.2:c.958-76T>A NP_570122.1:n.958-76T>A
XM_005256683.2:c.958-76T>A XP_005256740.1:n.958-76T>A
XM_005256685.1:c.910-76T>A XP_005256742.1:n.910-76T>A
XM_005256686.1:c.910-76T>A XP_005256743.1:n.910-76T>A
XM_011523934.1:c.958-76T>A XP_011522236.1:n.958-76T>A
XM_011523935.1:c.958-76T>A XP_011522237.1:n.958-76T>A
XM_011523936.1:c.781-76T>A XP_011522238.1:n.781-76T>A
XM_005256686.2:c.910-76T>A XP_005256743.1:n.910-76T>A
XM_011523936.2:c.781-76T>A XP_011522238.1:n.781-76T>A
XM_017024756.1:c.958-76T>A XP_016880245.1:n.958-76T>A
XM_017024757.2:c.910-76T>A XP_016880246.1:n.910-76T>A
XM_017024758.2:c.781-76T>A XP_016880247.1:n.781-76T>A
XM_017024759.1:c.781-76T>A XP_016880248.1:n.781-76T>A
XM_024450802.1:c.958-76T>A XP_024306570.1:n.958-76T>A
NM_016532.4:c.1186-76T>A MANE Select NP_057616.2:n.1186-76T>A
NM_001135642.2:c.958-76T>A NP_001129114.1:n.958-76T>A
NM_130766.3:c.958-76T>A NP_570122.1:n.958-76T>A