Canonical Allele Identifier: CA5337054
Community Standard Title: NM_019892.6(INPP5E):c.844G>A (p.Gly282Arg)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136434832C>T , CM000671.2:g.136434832C>T GRCh38
NC_000009.11:g.139329284C>T , CM000671.1:g.139329284C>T GRCh37
NC_000009.10:g.138449105C>T NCBI36
NG_016126.1:g.9973G>A

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.844G>A MANE Select NP_063945.2:p.Gly282Arg
ENST00000371712.4:c.844G>A MANE Select ENSP00000360777.3:p.Gly282Arg
NM_001318502.1:c.844G>A NP_001305431.1:p.Gly282Arg
NM_001318502.2:c.844G>A NP_001305431.1:p.Gly282Arg
NM_019892.4:c.844G>A NP_063945.2:p.Gly282Arg
NM_019892.5:c.844G>A NP_063945.2:p.Gly282Arg
ENST00000371712.3:c.844G>A ENSP00000360777.3:p.Gly282Arg
ENST00000674513.1:n.115G>A
ENST00000675256.1:c.32G>A
ENST00000676019.1:c.844G>A ENSP00000501984.1:p.Gly282Arg
XM_005266094.2:c.844G>A XP_005266151.1:p.Gly282Arg
XM_017014926.1:c.844G>A XP_016870415.1:p.Gly282Arg
XR_929828.1:n.1284G>A
XR_929828.2:n.1286G>A