Canonical Allele Identifier: CA1754594030
Gene: EN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461364A= , CM000669.2:g.155461364A= GRCh38
NC_000007.13:g.155254059A= , CM000669.1:g.155254059A= GRCh37
NC_000007.12:g.154946820A= NCBI36
NG_007124.1:g.9645A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297375.4:c.686-1007A= MANE Select ENSP00000297375.4:n.686-1007A=
NM_001427.3:c.686-1007A= NP_001418.2:n.686-1007A=
NM_001427.4:c.686-1007A= MANE Select NP_001418.2:n.686-1007A=