Canonical Allele Identifier: CA375565612
Community Standard Title: NM_019892.6(INPP5E):c.931C>T (p.Gln311Ter)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136434745G>A , CM000671.2:g.136434745G>A GRCh38
NC_000009.11:g.139329197G>A , CM000671.1:g.139329197G>A GRCh37
NC_000009.10:g.138449018G>A NCBI36
NG_016126.1:g.10060C>T

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.931C>T MANE Select NP_063945.2:p.Gln311Ter
ENST00000371712.4:c.931C>T MANE Select ENSP00000360777.3:p.Gln311Ter
NM_001318502.1:c.931C>T NP_001305431.1:p.Gln311Ter
NM_001318502.2:c.931C>T NP_001305431.1:p.Gln311Ter
NM_019892.4:c.931C>T NP_063945.2:p.Gln311Ter
NM_019892.5:c.931C>T NP_063945.2:p.Gln311Ter
ENST00000371712.3:c.931C>T ENSP00000360777.3:p.Gln311Ter
ENST00000674513.1:n.202C>T
ENST00000675256.1:c.119C>T
ENST00000676019.1:c.931C>T ENSP00000501984.1:p.Gln311Ter
XM_005266094.2:c.931C>T XP_005266151.1:p.Gln311Ter
XM_017014926.1:c.931C>T XP_016870415.1:p.Gln311Ter
XR_929828.1:n.1371C>T
XR_929828.2:n.1373C>T