Canonical Allele Identifier: CA2808185641

Gene: INPP5K

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1496173G>A , CM000679.2:g.1496173G>A	GRCh38
NC_000017.10:g.1399467G>A , CM000679.1:g.1399467G>A	GRCh37
NC_000017.9:g.1346217G>A	NCBI36
NG_029891.1:g.25716C>T
NG_047063.1:g.1535C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421807.7:c.1186-9C>T MANE Select	ENSP00000413937.2:n.1186-9C>T
ENST00000320345.10:c.958-9C>T	ENSP00000318476.6:n.958-9C>T
ENST00000350761.9:c.*777-9C>T	ENSP00000254712.5:n.*777-9C>T
ENST00000406424.8:c.958-9C>T	ENSP00000385177.4:n.958-9C>T
ENST00000421807.6:c.1186-9C>T	ENSP00000413937.2:n.1186-9C>T
ENST00000487039.1:n.289C>T
ENST00000574561.1:c.454-9C>T	ENSP00000461105.1:n.454-9C>T
NM_001135642.1:c.958-9C>T	NP_001129114.1:n.958-9C>T
NM_016532.3:c.1186-9C>T	NP_057616.2:n.1186-9C>T
NM_130766.2:c.958-9C>T	NP_570122.1:n.958-9C>T
XM_005256683.2:c.958-9C>T	XP_005256740.1:n.958-9C>T
XM_005256685.1:c.910-9C>T	XP_005256742.1:n.910-9C>T
XM_005256686.1:c.910-9C>T	XP_005256743.1:n.910-9C>T
XM_011523934.1:c.958-9C>T	XP_011522236.1:n.958-9C>T
XM_011523935.1:c.958-9C>T	XP_011522237.1:n.958-9C>T
XM_011523936.1:c.781-9C>T	XP_011522238.1:n.781-9C>T
XM_005256686.2:c.910-9C>T	XP_005256743.1:n.910-9C>T
XM_011523936.2:c.781-9C>T	XP_011522238.1:n.781-9C>T
XM_017024756.1:c.958-9C>T	XP_016880245.1:n.958-9C>T
XM_017024757.2:c.910-9C>T	XP_016880246.1:n.910-9C>T
XM_017024758.2:c.781-9C>T	XP_016880247.1:n.781-9C>T
XM_017024759.1:c.781-9C>T	XP_016880248.1:n.781-9C>T
XM_024450802.1:c.958-9C>T	XP_024306570.1:n.958-9C>T
NM_016532.4:c.1186-9C>T MANE Select	NP_057616.2:n.1186-9C>T
NM_001135642.2:c.958-9C>T	NP_001129114.1:n.958-9C>T
NM_130766.3:c.958-9C>T	NP_570122.1:n.958-9C>T