Canonical Allele Identifier: CA5337047
Community Standard Title: NM_019892.6(INPP5E):c.874C>G (p.Arg292Gly)
Gene: INPP5E HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.874C>G MANE Select NP_063945.2:p.Arg292Gly
ENST00000371712.4:c.874C>G MANE Select ENSP00000360777.3:p.Arg292Gly
NM_001318502.1:c.874C>G NP_001305431.1:p.Arg292Gly
NM_001318502.2:c.874C>G NP_001305431.1:p.Arg292Gly
NM_019892.4:c.874C>G NP_063945.2:p.Arg292Gly
NM_019892.5:c.874C>G NP_063945.2:p.Arg292Gly
ENST00000371712.3:c.874C>G ENSP00000360777.3:p.Arg292Gly
ENST00000674513.1:n.145C>G
ENST00000675256.1:c.62C>G
ENST00000676019.1:c.874C>G ENSP00000501984.1:p.Arg292Gly
XM_005266094.2:c.874C>G XP_005266151.1:p.Arg292Gly
XM_017014926.1:c.874C>G XP_016870415.1:p.Arg292Gly
XR_929828.1:n.1314C>G
XR_929828.2:n.1316C>G