Canonical Allele Identifier: CA375563549
Community Standard Title: NM_019892.6(INPP5E):c.1312G>A (p.Asp438Asn)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136432554C>T , CM000671.2:g.136432554C>T GRCh38
NC_000009.11:g.139327006C>T , CM000671.1:g.139327006C>T GRCh37
NC_000009.10:g.138446827C>T NCBI36
NG_016126.1:g.12251G>A

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.1312G>A MANE Select NP_063945.2:p.Asp438Asn
ENST00000371712.4:c.1312G>A MANE Select ENSP00000360777.3:p.Asp438Asn
NM_001318502.1:c.1309G>A NP_001305431.1:p.Asp437Asn
NM_001318502.2:c.1309G>A NP_001305431.1:p.Asp437Asn
NM_019892.4:c.1312G>A NP_063945.2:p.Asp438Asn
NM_019892.5:c.1312G>A NP_063945.2:p.Asp438Asn
ENST00000371712.3:c.1312G>A ENSP00000360777.3:p.Asp438Asn
ENST00000676019.1:c.1210G>A ENSP00000501984.1:p.Asp404Asn
XM_005266094.2:c.1309G>A XP_005266151.1:p.Asp437Asn
XM_017014926.1:c.1312G>A XP_016870415.1:p.Asp438Asn
XR_929828.1:n.1752G>A
XR_929828.2:n.1754G>A