Canonical Allele Identifier: CA2685784376
Gene: EN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155463309_155463353del , CM000669.2:g.155463309_155463353del GRCh38
NC_000007.13:g.155256004_155256048del , CM000669.1:g.155256004_155256048del GRCh37
NC_000007.12:g.154948765_154948809del NCBI36
NG_007124.1:g.11590_11634del

Transcript Alleles

HGVS Amino-acid Change
ENST00000297375.4:c.*622_*666del MANE Select ENSP00000297375.4:n.*622_*666del
NM_001427.3:c.*622_*666del NP_001418.2:n.*622_*666del
NM_001427.4:c.*622_*666del MANE Select NP_001418.2:n.*622_*666del