Canonical Allele Identifier: CA375563278
Community Standard Title: NM_019892.6(INPP5E):c.1367A>C (p.Asn456Thr)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136432499T>G , CM000671.2:g.136432499T>G GRCh38
NC_000009.11:g.139326951T>G , CM000671.1:g.139326951T>G GRCh37
NC_000009.10:g.138446772T>G NCBI36
NG_016126.1:g.12306A>C

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.1367A>C MANE Select NP_063945.2:p.Asn456Thr
ENST00000371712.4:c.1367A>C MANE Select ENSP00000360777.3:p.Asn456Thr
NM_001318502.1:c.1364A>C NP_001305431.1:p.Asn455Thr
NM_001318502.2:c.1364A>C NP_001305431.1:p.Asn455Thr
NM_019892.4:c.1367A>C NP_063945.2:p.Asn456Thr
NM_019892.5:c.1367A>C NP_063945.2:p.Asn456Thr
ENST00000371712.3:c.1367A>C ENSP00000360777.3:p.Asn456Thr
ENST00000676019.1:c.1265A>C ENSP00000501984.1:p.Asn422Thr
XM_005266094.2:c.1364A>C XP_005266151.1:p.Asn455Thr
XM_017014926.1:c.1367A>C XP_016870415.1:p.Asn456Thr
XR_929828.1:n.1807A>C
XR_929828.2:n.1809A>C