Canonical Allele Identifier: CA578797154
Gene: EN2 HGNC NCBI

Linked Data

dbSNP Id: rs1411597753
gnomAD v2: 7-155253869-T-TG
gnomAD v3: 7-155461174-T-TG
gnomAD v4: 7-155461174-T-TG
MyVariant Identifiers: chr7:g.155253869_155253870insG (hg19) chr7:g.155461174_155461175insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461180dup , CM000669.2:g.155461180dup GRCh38
NC_000007.13:g.155253875dup , CM000669.1:g.155253875dup GRCh37
NC_000007.12:g.154946636dup NCBI36
NG_007124.1:g.9461dup

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-1191dup MANE Select ENSP00000297375.4:n.686-1191dup
NM_001427.3:c.686-1191dup NP_001418.2:n.686-1191dup
NM_001427.4:c.686-1191dup MANE Select NP_001418.2:n.686-1191dup
Search 100 bp 5'
Search 100 bp 3'