Canonical Allele Identifier: CA5336729
Community Standard Title: NM_019892.6(INPP5E):c.1550-14C>T
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136431131G>A , CM000671.2:g.136431131G>A GRCh38
NC_000009.11:g.139325583G>A , CM000671.1:g.139325583G>A GRCh37
NC_000009.10:g.138445404G>A NCBI36
NG_016126.1:g.13674C>T

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.1550-14C>T MANE Select NP_063945.2:n.1550-14C>T
ENST00000371712.4:c.1550-14C>T MANE Select ENSP00000360777.3:n.1550-14C>T
NM_001318502.1:c.1547-14C>T NP_001305431.1:n.1547-14C>T
NM_001318502.2:c.1547-14C>T NP_001305431.1:n.1547-14C>T
NM_019892.4:c.1550-14C>T NP_063945.2:n.1550-14C>T
NM_019892.5:c.1550-14C>T NP_063945.2:n.1550-14C>T
ENST00000371712.3:c.1550-14C>T ENSP00000360777.3:n.1550-14C>T
ENST00000674693.1:n.53C>T
ENST00000676019.1:c.1448-14C>T ENSP00000501984.1:n.1448-14C>T
XM_005266094.2:c.1547-14C>T XP_005266151.1:n.1547-14C>T
XM_017014926.1:c.1550-14C>T XP_016870415.1:n.1550-14C>T
XR_929828.2:n.2155-14C>T