Canonical Allele Identifier: CA1754594005
Gene: EN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461310_155461313delinsCCTT , CM000669.2:g.155461310_155461313delinsCCTT GRCh38
NC_000007.13:g.155254005_155254008delinsCCTT , CM000669.1:g.155254005_155254008delinsCCTT GRCh37
NC_000007.12:g.154946766_154946769delinsCCTT NCBI36
NG_007124.1:g.9591_9594delinsCCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-1061_686-1058delinsCCTT MANE Select ENSP00000297375.4:n.686-1061_686-1058deli...
NM_001427.3:c.686-1061_686-1058delinsCCTT NP_001418.2:n.686-1061_686-1058delinsCCTT...
NM_001427.4:c.686-1061_686-1058delinsCCTT MANE Select NP_001418.2:n.686-1061_686-1058delinsCCTT...