Canonical Allele Identifier: CA381723774
Gene: INPPL1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.72230145G>A , CM000673.2:g.72230145G>A GRCh38
NC_000011.9:g.71941189G>A , CM000673.1:g.71941189G>A GRCh37
NC_000011.8:g.71618837G>A NCBI36
NG_023253.1:g.10308G>A
NG_023253.2:g.10308G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298229.7:c.964G>A MANE Select ENSP00000298229.2:p.Asp322Asn
ENST00000298229.6:c.964G>A ENSP00000298229.2:p.Asp322Asn
ENST00000538751.5:c.238G>A ENSP00000444619.1:p.Asp80Asn
ENST00000540329.5:c.148G>A ENSP00000440018.1:p.Asp50Asn
ENST00000541756.5:c.766G>A ENSP00000446360.2:p.Asp256Asn
NM_001567.3:c.964G>A NP_001558.3:p.Asp322Asn
XM_005273978.3:c.1030G>A XP_005274035.1:p.Asp344Asn
XM_005273979.3:c.1030G>A XP_005274036.1:p.Asp344Asn
XM_011544999.1:c.964G>A XP_011543301.1:p.Asp322Asn
XM_011545000.1:c.1030G>A XP_011543302.1:p.Asp344Asn
XM_005273979.4:c.1030G>A XP_005274036.1:p.Asp344Asn
XM_011544999.2:c.964G>A XP_011543301.1:p.Asp322Asn
XM_024448501.1:c.1030G>A XP_024304269.1:p.Asp344Asn
XM_024448502.1:c.1030G>A XP_024304270.1:p.Asp344Asn
XM_024448503.1:c.1000G>A XP_024304271.1:p.Asp334Asn
XM_024448504.1:c.964G>A XP_024304272.1:p.Asp322Asn
XM_024448505.1:c.1030G>A XP_024304273.1:p.Asp344Asn
NM_001567.4:c.964G>A MANE Select NP_001558.3:p.Asp322Asn