Canonical Allele Identifier: CA2242889245

Gene: INPP5K

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1495975_1495976delinsCG , CM000679.2:g.1495975_1495976delinsCG	GRCh38
NC_000017.10:g.1399269_1399270delinsCG , CM000679.1:g.1399269_1399270delinsCG	GRCh37
NC_000017.9:g.1346019_1346020delinsCG	NCBI36
NG_029891.1:g.25913_25914delinsCG
NG_047063.1:g.1732_1733delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421807.7:c.1290+84_1290+85delinsCG MANE Select	ENSP00000413937.2:n.1290+84_1290+85delinsCG
ENST00000320345.10:c.1062+84_1062+85delinsCG	ENSP00000318476.6:n.1062+84_1062+85delinsCG
ENST00000350761.9:c.*881+84_*881+85delinsCG	ENSP00000254712.5:n.*881+84_*881+85delinsCG
ENST00000406424.8:c.1062+84_1062+85delinsCG	ENSP00000385177.4:n.1062+84_1062+85delinsCG
ENST00000421807.6:c.1290+84_1290+85delinsCG	ENSP00000413937.2:n.1290+84_1290+85delinsCG
ENST00000487039.1:n.402+84_402+85delinsCG
NM_001135642.1:c.1062+84_1062+85delinsCG	NP_001129114.1:n.1062+84_1062+85delinsCG
NM_016532.3:c.1290+84_1290+85delinsCG	NP_057616.2:n.1290+84_1290+85delinsCG
NM_130766.2:c.1062+84_1062+85delinsCG	NP_570122.1:n.1062+84_1062+85delinsCG
XM_005256683.2:c.1062+84_1062+85delinsCG	XP_005256740.1:n.1062+84_1062+85delinsCG
XM_005256685.1:c.1014+84_1014+85delinsCG	XP_005256742.1:n.1014+84_1014+85delinsCG
XM_005256686.1:c.1014+84_1014+85delinsCG	XP_005256743.1:n.1014+84_1014+85delinsCG
XM_011523934.1:c.1062+84_1062+85delinsCG	XP_011522236.1:n.1062+84_1062+85delinsCG
XM_011523935.1:c.1062+84_1062+85delinsCG	XP_011522237.1:n.1062+84_1062+85delinsCG
XM_011523936.1:c.885+84_885+85delinsCG	XP_011522238.1:n.885+84_885+85delinsCG
XM_005256686.2:c.1014+84_1014+85delinsCG	XP_005256743.1:n.1014+84_1014+85delinsCG
XM_011523936.2:c.885+84_885+85delinsCG	XP_011522238.1:n.885+84_885+85delinsCG
XM_017024756.1:c.1062+84_1062+85delinsCG	XP_016880245.1:n.1062+84_1062+85delinsCG
XM_017024757.2:c.1014+84_1014+85delinsCG	XP_016880246.1:n.1014+84_1014+85delinsCG
XM_017024758.2:c.885+84_885+85delinsCG	XP_016880247.1:n.885+84_885+85delinsCG
XM_017024759.1:c.885+84_885+85delinsCG	XP_016880248.1:n.885+84_885+85delinsCG
XM_024450802.1:c.1062+84_1062+85delinsCG	XP_024306570.1:n.1062+84_1062+85delinsCG
NM_016532.4:c.1290+84_1290+85delinsCG MANE Select	NP_057616.2:n.1290+84_1290+85delinsCG
NM_001135642.2:c.1062+84_1062+85delinsCG	NP_001129114.1:n.1062+84_1062+85delinsCG
NM_130766.3:c.1062+84_1062+85delinsCG	NP_570122.1:n.1062+84_1062+85delinsCG