Canonical Allele Identifier: CA5336827
Community Standard Title: NM_019892.6(INPP5E):c.1387+19C>T
Gene: INPP5E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136432460G>A , CM000671.2:g.136432460G>A GRCh38
NC_000009.11:g.139326912G>A , CM000671.1:g.139326912G>A GRCh37
NC_000009.10:g.138446733G>A NCBI36
NG_016126.1:g.12345C>T

Transcript Alleles

HGVS Amino-acid Change
NM_019892.6:c.1387+19C>T MANE Select NP_063945.2:n.1387+19C>T
ENST00000371712.4:c.1387+19C>T MANE Select ENSP00000360777.3:n.1387+19C>T
NM_001318502.1:c.1384+19C>T NP_001305431.1:n.1384+19C>T
NM_001318502.2:c.1384+19C>T NP_001305431.1:n.1384+19C>T
NM_019892.4:c.1387+19C>T NP_063945.2:n.1387+19C>T
NM_019892.5:c.1387+19C>T NP_063945.2:n.1387+19C>T
ENST00000371712.3:c.1387+19C>T ENSP00000360777.3:n.1387+19C>T
ENST00000676019.1:c.1285+19C>T ENSP00000501984.1:n.1285+19C>T
XM_005266094.2:c.1384+19C>T XP_005266151.1:n.1384+19C>T
XM_017014926.1:c.1387+19C>T XP_016870415.1:n.1387+19C>T
XR_929828.1:n.1846C>T
XR_929828.2:n.1848C>T