Canonical Allele Identifier: CA918171129
Gene: EN2 HGNC NCBI

Linked Data

dbSNP Id: rs1563075490
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461185del , CM000669.2:g.155461185del GRCh38
NC_000007.13:g.155253880del , CM000669.1:g.155253880del GRCh37
NC_000007.12:g.154946641del NCBI36
NG_007124.1:g.9466del

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-1186del MANE Select ENSP00000297375.4:n.686-1186del
NM_001427.3:c.686-1186del NP_001418.2:n.686-1186del
NM_001427.4:c.686-1186del MANE Select NP_001418.2:n.686-1186del
Search 100 bp 5'
Search 100 bp 3'