Canonical Allele Identifier: CA6169884
Gene: INPPL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3031115
ClinVar RCV Id: RCV003892279
dbSNP Id: rs748457346

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72230264C>T , CM000673.2:g.72230264C>T GRCh38
NC_000011.9:g.71941308C>T , CM000673.1:g.71941308C>T GRCh37
NC_000011.8:g.71618956C>T NCBI36
NG_023253.1:g.10427C>T
NG_023253.2:g.10427C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000298229.7:c.1083C>T MANE Select ENSP00000298229.2:p.His361=
ENST00000298229.6:c.1083C>T ENSP00000298229.2:p.His361=
ENST00000538751.5:c.357C>T ENSP00000444619.1:p.His119=
ENST00000540329.5:c.267C>T ENSP00000440018.1:p.His89=
ENST00000541756.5:c.885C>T ENSP00000446360.2:p.His295=
NM_001567.3:c.1083C>T NP_001558.3:p.His361=
XM_005273978.3:c.1149C>T XP_005274035.1:p.His383=
XM_005273979.3:c.1149C>T XP_005274036.1:p.His383=
XM_011544999.1:c.1083C>T XP_011543301.1:p.His361=
XM_011545000.1:c.1149C>T XP_011543302.1:p.His383=
XM_005273979.4:c.1149C>T XP_005274036.1:p.His383=
XM_011544999.2:c.1083C>T XP_011543301.1:p.His361=
XM_024448501.1:c.1149C>T XP_024304269.1:p.His383=
XM_024448502.1:c.1149C>T XP_024304270.1:p.His383=
XM_024448503.1:c.1119C>T XP_024304271.1:p.His373=
XM_024448504.1:c.1083C>T XP_024304272.1:p.His361=
XM_024448505.1:c.1149C>T XP_024304273.1:p.His383=
NM_001567.4:c.1083C>T MANE Select NP_001558.3:p.His361=