Canonical Allele Identifier: CA1485062879
Gene: ENPEP HGNC NCBI

Linked Data

dbSNP Id: rs1723765702

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.110460488_110460489insAAAAACT , CM000666.2:g.110460488_110460489insAAAAACT GRCh38
NC_000004.11:g.111381644_111381645insAAAAACT , CM000666.1:g.111381644_111381645insAAAAACT GRCh37
NC_000004.10:g.111601093_111601094insAAAAACT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000510961.1:n.73-28053_73-28052insAAAAACT