Canonical Allele Identifier: CA497278598

Gene: INPP5K

Linked Data

• MyVariant Identifiers: chr17:g.1399354C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1496060C>T , CM000679.2:g.1496060C>T	GRCh38
NC_000017.10:g.1399354C>T , CM000679.1:g.1399354C>T	GRCh37
NC_000017.9:g.1346104C>T	NCBI36
NG_029891.1:g.25829G>A
NG_047063.1:g.1648G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421807.7:c.1290G>A MANE Select	ENSP00000413937.2:p.Gln430=
ENST00000320345.10:c.1062G>A	ENSP00000318476.6:p.Gln354=
ENST00000350761.9:c.*881G>A	ENSP00000254712.5:n.*881G>A
ENST00000406424.8:c.1062G>A	ENSP00000385177.4:p.Gln354=
ENST00000421807.6:c.1290G>A	ENSP00000413937.2:p.Gln430=
ENST00000487039.1:n.402G>A
NM_001135642.1:c.1062G>A	NP_001129114.1:p.Gln354=
NM_016532.3:c.1290G>A	NP_057616.2:p.Gln430=
NM_130766.2:c.1062G>A	NP_570122.1:p.Gln354=
XM_005256683.2:c.1062G>A	XP_005256740.1:p.Gln354=
XM_005256685.1:c.1014G>A	XP_005256742.1:p.Gln338=
XM_005256686.1:c.1014G>A	XP_005256743.1:p.Gln338=
XM_011523934.1:c.1062G>A	XP_011522236.1:p.Gln354=
XM_011523935.1:c.1062G>A	XP_011522237.1:p.Gln354=
XM_011523936.1:c.885G>A	XP_011522238.1:p.Gln295=
XM_005256686.2:c.1014G>A	XP_005256743.1:p.Gln338=
XM_011523936.2:c.885G>A	XP_011522238.1:p.Gln295=
XM_017024756.1:c.1062G>A	XP_016880245.1:p.Gln354=
XM_017024757.2:c.1014G>A	XP_016880246.1:p.Gln338=
XM_017024758.2:c.885G>A	XP_016880247.1:p.Gln295=
XM_017024759.1:c.885G>A	XP_016880248.1:p.Gln295=
XM_024450802.1:c.1062G>A	XP_024306570.1:p.Gln354=
NM_016532.4:c.1290G>A MANE Select	NP_057616.2:p.Gln430=
NM_001135642.2:c.1062G>A	NP_001129114.1:p.Gln354=
NM_130766.3:c.1062G>A	NP_570122.1:p.Gln354=