Canonical Allele Identifier: CA5337045
Community Standard Title: NM_019892.6(INPP5E):c.878A>T (p.Tyr293Phe)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136434798T>A , CM000671.2:g.136434798T>A GRCh38
NC_000009.11:g.139329250T>A , CM000671.1:g.139329250T>A GRCh37
NC_000009.10:g.138449071T>A NCBI36
NG_016126.1:g.10007A>T

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.878A>T MANE Select NP_063945.2:p.Tyr293Phe
ENST00000371712.4:c.878A>T MANE Select ENSP00000360777.3:p.Tyr293Phe
NM_001318502.1:c.878A>T NP_001305431.1:p.Tyr293Phe
NM_001318502.2:c.878A>T NP_001305431.1:p.Tyr293Phe
NM_019892.4:c.878A>T NP_063945.2:p.Tyr293Phe
NM_019892.5:c.878A>T NP_063945.2:p.Tyr293Phe
ENST00000371712.3:c.878A>T ENSP00000360777.3:p.Tyr293Phe
ENST00000674513.1:n.149A>T
ENST00000675256.1:c.66A>T
ENST00000676019.1:c.878A>T ENSP00000501984.1:p.Tyr293Phe
XM_005266094.2:c.878A>T XP_005266151.1:p.Tyr293Phe
XM_017014926.1:c.878A>T XP_016870415.1:p.Tyr293Phe
XR_929828.1:n.1318A>T
XR_929828.2:n.1320A>T