Canonical Allele Identifier: CA2778551040
Gene: EN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461366C>A , CM000669.2:g.155461366C>A GRCh38
NC_000007.13:g.155254061C>A , CM000669.1:g.155254061C>A GRCh37
NC_000007.12:g.154946822C>A NCBI36
NG_007124.1:g.9647C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297375.4:c.686-1005C>A MANE Select ENSP00000297375.4:n.686-1005C>A
NM_001427.3:c.686-1005C>A NP_001418.2:n.686-1005C>A
NM_001427.4:c.686-1005C>A MANE Select NP_001418.2:n.686-1005C>A