Canonical Allele Identifier: CA1754593984
Gene: EN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461271_155461272delinsCA , CM000669.2:g.155461271_155461272delinsCA GRCh38
NC_000007.13:g.155253966_155253967delinsCA , CM000669.1:g.155253966_155253967delinsCA GRCh37
NC_000007.12:g.154946727_154946728delinsCA NCBI36
NG_007124.1:g.9552_9553delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-1100_686-1099delinsCA MANE Select ENSP00000297375.4:n.686-1100_686-1099deli...
NM_001427.3:c.686-1100_686-1099delinsCA NP_001418.2:n.686-1100_686-1099delinsCA
NM_001427.4:c.686-1100_686-1099delinsCA MANE Select NP_001418.2:n.686-1100_686-1099delinsCA