Canonical Allele Identifier: CA397536177
Gene: INPP5K HGNC NCBI

Linked Data

dbSNP Id: rs754331645
gnomAD v2: 17-1399399-G-C
gnomAD v3: 17-1496105-G-C
gnomAD v4: 17-1496105-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1496105G>C , CM000679.2:g.1496105G>C GRCh38
NC_000017.10:g.1399399G>C , CM000679.1:g.1399399G>C GRCh37
NC_000017.9:g.1346149G>C NCBI36
NG_029891.1:g.25784C>G
NG_047063.1:g.1603C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000421807.7:c.1245C>G MANE Select ENSP00000413937.2:p.Tyr415Ter
ENST00000320345.10:c.1017C>G ENSP00000318476.6:p.Tyr339Ter
ENST00000350761.9:c.*836C>G ENSP00000254712.5:n.*836C>G
ENST00000406424.8:c.1017C>G ENSP00000385177.4:p.Tyr339Ter
ENST00000421807.6:c.1245C>G ENSP00000413937.2:p.Tyr415Ter
ENST00000487039.1:n.357C>G
NM_001135642.1:c.1017C>G NP_001129114.1:p.Tyr339Ter
NM_016532.3:c.1245C>G NP_057616.2:p.Tyr415Ter
NM_130766.2:c.1017C>G NP_570122.1:p.Tyr339Ter
XM_005256683.2:c.1017C>G XP_005256740.1:p.Tyr339Ter
XM_005256685.1:c.969C>G XP_005256742.1:p.Tyr323Ter
XM_005256686.1:c.969C>G XP_005256743.1:p.Tyr323Ter
XM_011523934.1:c.1017C>G XP_011522236.1:p.Tyr339Ter
XM_011523935.1:c.1017C>G XP_011522237.1:p.Tyr339Ter
XM_011523936.1:c.840C>G XP_011522238.1:p.Tyr280Ter
XM_005256686.2:c.969C>G XP_005256743.1:p.Tyr323Ter
XM_011523936.2:c.840C>G XP_011522238.1:p.Tyr280Ter
XM_017024756.1:c.1017C>G XP_016880245.1:p.Tyr339Ter
XM_017024757.2:c.969C>G XP_016880246.1:p.Tyr323Ter
XM_017024758.2:c.840C>G XP_016880247.1:p.Tyr280Ter
XM_017024759.1:c.840C>G XP_016880248.1:p.Tyr280Ter
XM_024450802.1:c.1017C>G XP_024306570.1:p.Tyr339Ter
NM_016532.4:c.1245C>G MANE Select NP_057616.2:p.Tyr415Ter
NM_001135642.2:c.1017C>G NP_001129114.1:p.Tyr339Ter
NM_130766.3:c.1017C>G NP_570122.1:p.Tyr339Ter