Canonical Allele Identifier: CA10587060
Community Standard Title: NM_019892.6(INPP5E):c.1543C>A (p.Arg515=)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136431830G>T , CM000671.2:g.136431830G>T GRCh38
NC_000009.11:g.139326282G>T , CM000671.1:g.139326282G>T GRCh37
NC_000009.10:g.138446103G>T NCBI36
NG_016126.1:g.12975C>A

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.1543C>A MANE Select NP_063945.2:p.Arg515=
ENST00000371712.4:c.1543C>A MANE Select ENSP00000360777.3:p.Arg515=
NM_001318502.1:c.1540C>A NP_001305431.1:p.Arg514=
NM_001318502.2:c.1540C>A NP_001305431.1:p.Arg514=
NM_019892.4:c.1543C>A NP_063945.2:p.Arg515=
NM_019892.5:c.1543C>A NP_063945.2:p.Arg515=
ENST00000371712.3:c.1543C>A ENSP00000360777.3:p.Arg515=
ENST00000676019.1:c.1441C>A ENSP00000501984.1:p.Arg481=
XM_005266094.2:c.1540C>A XP_005266151.1:p.Arg514=
XM_017014926.1:c.1543C>A XP_016870415.1:p.Arg515=
XR_929828.2:n.2148C>A