Canonical Allele Identifier: CA201638643
Community Standard Title: NM_019892.6(INPP5E):c.1615G>A (p.Gly539Arg)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136431052C>T , CM000671.2:g.136431052C>T GRCh38
NC_000009.11:g.139325504C>T , CM000671.1:g.139325504C>T GRCh37
NC_000009.10:g.138445325C>T NCBI36
NG_016126.1:g.13753G>A

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.1615G>A MANE Select NP_063945.2:p.Gly539Arg
ENST00000371712.4:c.1615G>A MANE Select ENSP00000360777.3:p.Gly539Arg
NM_001318502.1:c.1612G>A NP_001305431.1:p.Gly538Arg
NM_001318502.2:c.1612G>A NP_001305431.1:p.Gly538Arg
NM_019892.4:c.1615G>A NP_063945.2:p.Gly539Arg
NM_019892.5:c.1615G>A NP_063945.2:p.Gly539Arg
ENST00000371712.3:c.1615G>A ENSP00000360777.3:p.Gly539Arg
ENST00000674693.1:n.132G>A
ENST00000676019.1:c.1513G>A ENSP00000501984.1:p.Gly505Arg
XM_005266094.2:c.1612G>A XP_005266151.1:p.Gly538Arg
XM_017014926.1:c.1615G>A XP_016870415.1:p.Gly539Arg
XR_929828.2:n.2220G>A