Canonical Allele Identifier: CA2685784296
Gene: EN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155463223del , CM000669.2:g.155463223del GRCh38
NC_000007.13:g.155255918del , CM000669.1:g.155255918del GRCh37
NC_000007.12:g.154948679del NCBI36
NG_007124.1:g.11504del

Transcript Alleles

HGVS Amino-acid Change
ENST00000297375.4:c.*536del MANE Select ENSP00000297375.4:n.*536del
NM_001427.3:c.*536del NP_001418.2:n.*536del
NM_001427.4:c.*536del MANE Select NP_001418.2:n.*536del