Canonical Allele Identifier: CA201638363
Community Standard Title: NM_019892.6(INPP5E):c.1670G>A (p.Arg557His)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136430409C>T , CM000671.2:g.136430409C>T GRCh38
NC_000009.11:g.139324861C>T , CM000671.1:g.139324861C>T GRCh37
NC_000009.10:g.138444682C>T NCBI36
NG_016126.1:g.14396G>A

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.1670G>A MANE Select NP_063945.2:p.Arg557His
ENST00000371712.4:c.1670G>A MANE Select ENSP00000360777.3:p.Arg557His
NM_001318502.1:c.1667G>A NP_001305431.1:p.Arg556His
NM_001318502.2:c.1667G>A NP_001305431.1:p.Arg556His
NM_019892.4:c.1670G>A NP_063945.2:p.Arg557His
NM_019892.5:c.1670G>A NP_063945.2:p.Arg557His
ENST00000371712.3:c.1670G>A ENSP00000360777.3:p.Arg557His
ENST00000674693.1:n.187G>A
ENST00000676019.1:c.1568G>A ENSP00000501984.1:p.Arg523His
XM_005266094.2:c.1667G>A XP_005266151.1:p.Arg556His
XM_017014926.1:c.1670G>A XP_016870415.1:p.Arg557His
XR_929828.2:n.2275G>A