Canonical Allele Identifier: CA2692606179
Gene: INPP5E HGNC NCBI

Linked Data

gnomAD v4: 9-136428773-C-G
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000371712.4:c.*902G>C MANE Select ENSP00000360777.3:n.*902G>C
ENST00000676019.1:c.*902G>C ENSP00000501984.1:n.*902G>C
ENST00000371712.3:c.*902G>C ENSP00000360777.3:n.*902G>C
NM_019892.4:c.*902G>C NP_063945.2:n.*902G>C
XM_005266094.2:c.*902G>C XP_005266151.1:n.*902G>C
NM_001318502.1:c.*902G>C NP_001305431.1:n.*902G>C
NM_019892.5:c.*902G>C NP_063945.2:n.*902G>C
XM_017014926.1:c.*981G>C XP_016870415.1:n.*981G>C
NM_019892.6:c.*902G>C MANE Select NP_063945.2:n.*902G>C
NM_001318502.2:c.*902G>C NP_001305431.1:n.*902G>C
Search 100 bp 5'
Search 100 bp 3'