Canonical Allele Identifier: CA2242898379
Gene: INPP5K HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1513875A= , CM000679.2:g.1513875A= GRCh38
NC_000017.10:g.1417169A= , CM000679.1:g.1417169A= GRCh37
NC_000017.9:g.1363919A= NCBI36
NG_029891.1:g.8014T=

Transcript Alleles

HGVS Amino-acid change
ENST00000421807.7:c.149T= MANE Select ENSP00000413937.2:p.Ile50=
ENST00000320345.10:c.-80T= ENSP00000318476.6:n.-80T=
ENST00000350761.9:c.44+2581T= ENSP00000254712.5:n.44+2581T=
ENST00000406424.8:c.-80T= ENSP00000385177.4:n.-80T=
ENST00000421807.6:c.149T= ENSP00000413937.2:p.Ile50=
ENST00000445774.2:c.149T= ENSP00000389334.2:p.Ile50=
ENST00000449479.5:c.-19T= ENSP00000413259.1:n.-19T=
ENST00000477910.5:c.-80T= ENSP00000467376.1:n.-80T=
ENST00000498390.5:c.-19T= ENSP00000466929.1:n.-19T=
ENST00000571274.5:c.-80T= ENSP00000458413.1:n.-80T=
ENST00000573790.5:c.149T= ENSP00000461846.1:p.Ile50=
ENST00000574561.1:c.44+2581T= ENSP00000461105.1:n.44+2581T=
ENST00000574955.1:c.*152T= ENSP00000459029.1:n.*152T=
ENST00000575172.5:c.149T= ENSP00000459758.1:p.Ile50=
ENST00000576646.7:c.105T=
NM_001135642.1:c.-80T= NP_001129114.1:n.-80T=
NM_016532.3:c.149T= NP_057616.2:p.Ile50=
NM_130766.2:c.-80T= NP_570122.1:n.-80T=
XM_005256683.2:c.-73T= XP_005256740.1:n.-73T=
XM_005256685.1:c.-19T= XP_005256742.1:n.-19T=
XM_005256686.1:c.-19T= XP_005256743.1:n.-19T=
XM_011523934.1:c.-80T= XP_011522236.1:n.-80T=
XM_011523935.1:c.-80T= XP_011522237.1:n.-80T=
XM_011523936.1:c.-260T= XP_011522238.1:n.-260T=
XM_005256686.2:c.-19T= XP_005256743.1:n.-19T=
XM_011523936.2:c.-260T= XP_011522238.1:n.-260T=
XM_017024756.1:c.-73T= XP_016880245.1:n.-73T=
XM_017024757.2:c.-19T= XP_016880246.1:n.-19T=
XM_017024758.2:c.-267T= XP_016880247.1:n.-267T=
XM_017024759.1:c.-158T= XP_016880248.1:n.-158T=
XM_024450802.1:c.-73T= XP_024306570.1:n.-73T=
NM_016532.4:c.149T= MANE Select NP_057616.2:p.Ile50=
NM_001135642.2:c.-80T= NP_001129114.1:n.-80T=
NM_130766.3:c.-80T= NP_570122.1:n.-80T=