Canonical Allele Identifier: CA375565914
Community Standard Title: NM_019892.6(INPP5E):c.874C>T (p.Arg292Cys)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136434802G>A , CM000671.2:g.136434802G>A GRCh38
NC_000009.11:g.139329254G>A , CM000671.1:g.139329254G>A GRCh37
NC_000009.10:g.138449075G>A NCBI36
NG_016126.1:g.10003C>T

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.874C>T MANE Select NP_063945.2:p.Arg292Cys
ENST00000371712.4:c.874C>T MANE Select ENSP00000360777.3:p.Arg292Cys
NM_001318502.1:c.874C>T NP_001305431.1:p.Arg292Cys
NM_001318502.2:c.874C>T NP_001305431.1:p.Arg292Cys
NM_019892.4:c.874C>T NP_063945.2:p.Arg292Cys
NM_019892.5:c.874C>T NP_063945.2:p.Arg292Cys
ENST00000371712.3:c.874C>T ENSP00000360777.3:p.Arg292Cys
ENST00000674513.1:n.145C>T
ENST00000675256.1:c.62C>T
ENST00000676019.1:c.874C>T ENSP00000501984.1:p.Arg292Cys
XM_005266094.2:c.874C>T XP_005266151.1:p.Arg292Cys
XM_017014926.1:c.874C>T XP_016870415.1:p.Arg292Cys
XR_929828.1:n.1314C>T
XR_929828.2:n.1316C>T