Canonical Allele Identifier: CA1754593951
Gene: EN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461194C= , CM000669.2:g.155461194C= GRCh38
NC_000007.13:g.155253889C= , CM000669.1:g.155253889C= GRCh37
NC_000007.12:g.154946650C= NCBI36
NG_007124.1:g.9475C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297375.4:c.686-1177C= MANE Select ENSP00000297375.4:n.686-1177C=
NM_001427.3:c.686-1177C= NP_001418.2:n.686-1177C=
NM_001427.4:c.686-1177C= MANE Select NP_001418.2:n.686-1177C=