Canonical Allele Identifier: CA169340149
Gene: EN2 HGNC NCBI

Linked Data

dbSNP Id: rs35529773

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461311del , CM000669.2:g.155461311del GRCh38
NC_000007.13:g.155254006del , CM000669.1:g.155254006del GRCh37
NC_000007.12:g.154946767del NCBI36
NG_007124.1:g.9592del

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-1060del MANE Select ENSP00000297375.4:n.686-1060del
NM_001427.3:c.686-1060del NP_001418.2:n.686-1060del
NM_001427.4:c.686-1060del MANE Select NP_001418.2:n.686-1060del