Canonical Allele Identifier: CA1754594003
Gene: EN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461306_155461307delinsGC , CM000669.2:g.155461306_155461307delinsGC GRCh38
NC_000007.13:g.155254001_155254002delinsGC , CM000669.1:g.155254001_155254002delinsGC GRCh37
NC_000007.12:g.154946762_154946763delinsGC NCBI36
NG_007124.1:g.9587_9588delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-1065_686-1064delinsGC MANE Select ENSP00000297375.4:n.686-1065_686-1064deli...
NM_001427.3:c.686-1065_686-1064delinsGC NP_001418.2:n.686-1065_686-1064delinsGC
NM_001427.4:c.686-1065_686-1064delinsGC MANE Select NP_001418.2:n.686-1065_686-1064delinsGC