Canonical Allele Identifier: CA1754594020
Gene: EN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461340T= , CM000669.2:g.155461340T= GRCh38
NC_000007.13:g.155254035T= , CM000669.1:g.155254035T= GRCh37
NC_000007.12:g.154946796T= NCBI36
NG_007124.1:g.9621T=

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-1031T= MANE Select ENSP00000297375.4:n.686-1031T=
NM_001427.3:c.686-1031T= NP_001418.2:n.686-1031T=
NM_001427.4:c.686-1031T= MANE Select NP_001418.2:n.686-1031T=