Canonical Allele Identifier: CA2242898381

Gene: INPP5K

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1513882A= , CM000679.2:g.1513882A=	GRCh38
NC_000017.10:g.1417176A= , CM000679.1:g.1417176A=	GRCh37
NC_000017.9:g.1363926A=	NCBI36
NG_029891.1:g.8007T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000421807.7:c.142T= MANE Select	ENSP00000413937.2:p.Tyr48=
ENST00000320345.10:c.-87T=	ENSP00000318476.6:n.-87T=
ENST00000350761.9:c.44+2574T=	ENSP00000254712.5:n.44+2574T=
ENST00000406424.8:c.-87T=	ENSP00000385177.4:n.-87T=
ENST00000421807.6:c.142T=	ENSP00000413937.2:p.Tyr48=
ENST00000445774.2:c.142T=	ENSP00000389334.2:p.Tyr48=
ENST00000449479.5:c.-26T=	ENSP00000413259.1:n.-26T=
ENST00000477910.5:c.-87T=	ENSP00000467376.1:n.-87T=
ENST00000498390.5:c.-26T=	ENSP00000466929.1:n.-26T=
ENST00000571274.5:c.-87T=	ENSP00000458413.1:n.-87T=
ENST00000573790.5:c.142T=	ENSP00000461846.1:p.Tyr48=
ENST00000574561.1:c.44+2574T=	ENSP00000461105.1:n.44+2574T=
ENST00000574955.1:c.*145T=	ENSP00000459029.1:n.*145T=
ENST00000575172.5:c.142T=	ENSP00000459758.1:p.Tyr48=
ENST00000576646.7:c.98T=
NM_001135642.1:c.-87T=	NP_001129114.1:n.-87T=
NM_016532.3:c.142T=	NP_057616.2:p.Tyr48=
NM_130766.2:c.-87T=	NP_570122.1:n.-87T=
XM_005256683.2:c.-80T=	XP_005256740.1:n.-80T=
XM_005256685.1:c.-26T=	XP_005256742.1:n.-26T=
XM_005256686.1:c.-26T=	XP_005256743.1:n.-26T=
XM_011523934.1:c.-87T=	XP_011522236.1:n.-87T=
XM_011523935.1:c.-87T=	XP_011522237.1:n.-87T=
XM_011523936.1:c.-267T=	XP_011522238.1:n.-267T=
XM_005256686.2:c.-26T=	XP_005256743.1:n.-26T=
XM_011523936.2:c.-267T=	XP_011522238.1:n.-267T=
XM_017024756.1:c.-80T=	XP_016880245.1:n.-80T=
XM_017024757.2:c.-26T=	XP_016880246.1:n.-26T=
XM_017024758.2:c.-274T=	XP_016880247.1:n.-274T=
XM_017024759.1:c.-165T=	XP_016880248.1:n.-165T=
XM_024450802.1:c.-80T=	XP_024306570.1:n.-80T=
NM_016532.4:c.142T= MANE Select	NP_057616.2:p.Tyr48=
NM_001135642.2:c.-87T=	NP_001129114.1:n.-87T=
NM_130766.3:c.-87T=	NP_570122.1:n.-87T=