Canonical Allele Identifier: CA835662296
Gene: EN2 HGNC NCBI

Linked Data

dbSNP Id: rs1290119646
MyVariant Identifiers: chr7:g.155254078_155254080del (hg19) chr7:g.155461383_155461385del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461385_155461387del , CM000669.2:g.155461385_155461387del GRCh38
NC_000007.13:g.155254080_155254082del , CM000669.1:g.155254080_155254082del GRCh37
NC_000007.12:g.154946841_154946843del NCBI36
NG_007124.1:g.9666_9668del

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-986_686-984del MANE Select ENSP00000297375.4:n.686-986_686-984del
NM_001427.3:c.686-986_686-984del NP_001418.2:n.686-986_686-984del
NM_001427.4:c.686-986_686-984del MANE Select NP_001418.2:n.686-986_686-984del
Search 100 bp 5'
Search 100 bp 3'