Canonical Allele Identifier: CA1884222240
Gene: INPP5E HGNC NCBI

Linked Data

dbSNP Id: rs1835630730

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136428773C>T , CM000671.2:g.136428773C>T GRCh38
NC_000009.11:g.139323225C>T , CM000671.1:g.139323225C>T GRCh37
NC_000009.10:g.138443046C>T NCBI36
NG_016126.1:g.16032G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371712.4:c.*902G>A MANE Select ENSP00000360777.3:n.*902G>A
ENST00000676019.1:c.*902G>A ENSP00000501984.1:n.*902G>A
ENST00000371712.3:c.*902G>A ENSP00000360777.3:n.*902G>A
NM_019892.4:c.*902G>A NP_063945.2:n.*902G>A
XM_005266094.2:c.*902G>A XP_005266151.1:n.*902G>A
NM_001318502.1:c.*902G>A NP_001305431.1:n.*902G>A
NM_019892.5:c.*902G>A NP_063945.2:n.*902G>A
XM_017014926.1:c.*981G>A XP_016870415.1:n.*981G>A
NM_019892.6:c.*902G>A MANE Select NP_063945.2:n.*902G>A
NM_001318502.2:c.*902G>A NP_001305431.1:n.*902G>A