Canonical Allele Identifier: CA5337153
Community Standard Title: NM_019892.6(INPP5E):c.469G>T (p.Gly157Trp)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136438951C>A , CM000671.2:g.136438951C>A GRCh38
NC_000009.11:g.139333403C>A , CM000671.1:g.139333403C>A GRCh37
NC_000009.10:g.138453224C>A NCBI36
NG_016126.1:g.5854G>T

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.469G>T MANE Select NP_063945.2:p.Gly157Trp
ENST00000371712.4:c.469G>T MANE Select ENSP00000360777.3:p.Gly157Trp
NM_001318502.1:c.469G>T NP_001305431.1:p.Gly157Trp
NM_001318502.2:c.469G>T NP_001305431.1:p.Gly157Trp
NM_019892.4:c.469G>T NP_063945.2:p.Gly157Trp
NM_019892.5:c.469G>T NP_063945.2:p.Gly157Trp
ENST00000371712.3:c.469G>T ENSP00000360777.3:p.Gly157Trp
ENST00000635815.1:n.873G>T
ENST00000676019.1:c.469G>T ENSP00000501984.1:p.Gly157Trp
XM_005266094.2:c.469G>T XP_005266151.1:p.Gly157Trp
XM_017014926.1:c.469G>T XP_016870415.1:p.Gly157Trp
XR_929828.1:n.909G>T
XR_929828.2:n.911G>T