Canonical Allele Identifier: CA375561221
Community Standard Title: NM_019892.6(INPP5E):c.1747G>T (p.Asp583Tyr)
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136430332C>A , CM000671.2:g.136430332C>A GRCh38
NC_000009.11:g.139324784C>A , CM000671.1:g.139324784C>A GRCh37
NC_000009.10:g.138444605C>A NCBI36
NG_016126.1:g.14473G>T

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.1747G>T MANE Select NP_063945.2:p.Asp583Tyr
ENST00000371712.4:c.1747G>T MANE Select ENSP00000360777.3:p.Asp583Tyr
NM_001318502.1:c.1744G>T NP_001305431.1:p.Asp582Tyr
NM_001318502.2:c.1744G>T NP_001305431.1:p.Asp582Tyr
NM_019892.4:c.1747G>T NP_063945.2:p.Asp583Tyr
NM_019892.5:c.1747G>T NP_063945.2:p.Asp583Tyr
ENST00000371712.3:c.1747G>T ENSP00000360777.3:p.Asp583Tyr
ENST00000676019.1:c.1645G>T ENSP00000501984.1:p.Asp549Tyr
XM_005266094.2:c.1744G>T XP_005266151.1:p.Asp582Tyr
XM_017014926.1:c.1747G>T XP_016870415.1:p.Asp583Tyr
XR_929828.2:n.2352G>T