Canonical Allele Identifier: CA5337185
Community Standard Title: NM_019892.6(INPP5E):c.304G>T (p.Asp102Tyr)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136439116C>A , CM000671.2:g.136439116C>A GRCh38
NC_000009.11:g.139333568C>A , CM000671.1:g.139333568C>A GRCh37
NC_000009.10:g.138453389C>A NCBI36
NG_016126.1:g.5689G>T

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.304G>T MANE Select NP_063945.2:p.Asp102Tyr
ENST00000371712.4:c.304G>T MANE Select ENSP00000360777.3:p.Asp102Tyr
NM_001318502.1:c.304G>T NP_001305431.1:p.Asp102Tyr
NM_001318502.2:c.304G>T NP_001305431.1:p.Asp102Tyr
NM_019892.4:c.304G>T NP_063945.2:p.Asp102Tyr
NM_019892.5:c.304G>T NP_063945.2:p.Asp102Tyr
ENST00000371712.3:c.304G>T ENSP00000360777.3:p.Asp102Tyr
ENST00000635815.1:n.708G>T
ENST00000676019.1:c.304G>T ENSP00000501984.1:p.Asp102Tyr
XM_005266094.2:c.304G>T XP_005266151.1:p.Asp102Tyr
XM_017014926.1:c.304G>T XP_016870415.1:p.Asp102Tyr
XR_929828.1:n.744G>T
XR_929828.2:n.746G>T