Canonical Allele Identifier: CA397535440
Gene: INPP5K HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1495833G>C , CM000679.2:g.1495833G>C GRCh38
NC_000017.10:g.1399127G>C , CM000679.1:g.1399127G>C GRCh37
NC_000017.9:g.1345877G>C NCBI36
NG_029891.1:g.26056C>G
NG_047063.1:g.1875C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000421807.7:c.1337C>G MANE Select ENSP00000413937.2:p.Pro446Arg
ENST00000320345.10:c.1109C>G ENSP00000318476.6:p.Pro370Arg
ENST00000350761.9:c.*928C>G ENSP00000254712.5:n.*928C>G
ENST00000406424.8:c.1109C>G ENSP00000385177.4:p.Pro370Arg
ENST00000421807.6:c.1337C>G ENSP00000413937.2:p.Pro446Arg
ENST00000487039.1:n.449C>G
NM_001135642.1:c.1109C>G NP_001129114.1:p.Pro370Arg
NM_016532.3:c.1337C>G NP_057616.2:p.Pro446Arg
NM_130766.2:c.1109C>G NP_570122.1:p.Pro370Arg
XM_005256683.2:c.1109C>G XP_005256740.1:p.Pro370Arg
XM_005256685.1:c.1061C>G XP_005256742.1:p.Pro354Arg
XM_005256686.1:c.1061C>G XP_005256743.1:p.Pro354Arg
XM_011523934.1:c.1109C>G XP_011522236.1:p.Pro370Arg
XM_011523935.1:c.1109C>G XP_011522237.1:p.Pro370Arg
XM_011523936.1:c.932C>G XP_011522238.1:p.Pro311Arg
XM_005256686.2:c.1061C>G XP_005256743.1:p.Pro354Arg
XM_011523936.2:c.932C>G XP_011522238.1:p.Pro311Arg
XM_017024756.1:c.1109C>G XP_016880245.1:p.Pro370Arg
XM_017024757.2:c.1061C>G XP_016880246.1:p.Pro354Arg
XM_017024758.2:c.932C>G XP_016880247.1:p.Pro311Arg
XM_017024759.1:c.932C>G XP_016880248.1:p.Pro311Arg
XM_024450802.1:c.1109C>G XP_024306570.1:p.Pro370Arg
NM_016532.4:c.1337C>G MANE Select NP_057616.2:p.Pro446Arg
NM_001135642.2:c.1109C>G NP_001129114.1:p.Pro370Arg
NM_130766.3:c.1109C>G NP_570122.1:p.Pro370Arg