Canonical Allele Identifier: CA397536422

Gene: INPP5K

Linked Data

• gnomAD v4: 17-1496143-T-C
• MyVariant Identifiers: chr17:g.1399437T>C (hg19) ; chr17:g.1496143T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1496143T>C , CM000679.2:g.1496143T>C	GRCh38
NC_000017.10:g.1399437T>C , CM000679.1:g.1399437T>C	GRCh37
NC_000017.9:g.1346187T>C	NCBI36
NG_029891.1:g.25746A>G
NG_047063.1:g.1565A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421807.7:c.1207A>G MANE Select	ENSP00000413937.2:p.Ile403Val
ENST00000320345.10:c.979A>G	ENSP00000318476.6:p.Ile327Val
ENST00000350761.9:c.*798A>G	ENSP00000254712.5:n.*798A>G
ENST00000406424.8:c.979A>G	ENSP00000385177.4:p.Ile327Val
ENST00000421807.6:c.1207A>G	ENSP00000413937.2:p.Ile403Val
ENST00000487039.1:n.319A>G
NM_001135642.1:c.979A>G	NP_001129114.1:p.Ile327Val
NM_016532.3:c.1207A>G	NP_057616.2:p.Ile403Val
NM_130766.2:c.979A>G	NP_570122.1:p.Ile327Val
XM_005256683.2:c.979A>G	XP_005256740.1:p.Ile327Val
XM_005256685.1:c.931A>G	XP_005256742.1:p.Ile311Val
XM_005256686.1:c.931A>G	XP_005256743.1:p.Ile311Val
XM_011523934.1:c.979A>G	XP_011522236.1:p.Ile327Val
XM_011523935.1:c.979A>G	XP_011522237.1:p.Ile327Val
XM_011523936.1:c.802A>G	XP_011522238.1:p.Ile268Val
XM_005256686.2:c.931A>G	XP_005256743.1:p.Ile311Val
XM_011523936.2:c.802A>G	XP_011522238.1:p.Ile268Val
XM_017024756.1:c.979A>G	XP_016880245.1:p.Ile327Val
XM_017024757.2:c.931A>G	XP_016880246.1:p.Ile311Val
XM_017024758.2:c.802A>G	XP_016880247.1:p.Ile268Val
XM_017024759.1:c.802A>G	XP_016880248.1:p.Ile268Val
XM_024450802.1:c.979A>G	XP_024306570.1:p.Ile327Val
NM_016532.4:c.1207A>G MANE Select	NP_057616.2:p.Ile403Val
NM_001135642.2:c.979A>G	NP_001129114.1:p.Ile327Val
NM_130766.3:c.979A>G	NP_570122.1:p.Ile327Val