Canonical Allele Identifier: CA1754594038
Gene: EN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461380C= , CM000669.2:g.155461380C= GRCh38
NC_000007.13:g.155254075C= , CM000669.1:g.155254075C= GRCh37
NC_000007.12:g.154946836C= NCBI36
NG_007124.1:g.9661C=

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-991C= MANE Select ENSP00000297375.4:n.686-991C=
NM_001427.3:c.686-991C= NP_001418.2:n.686-991C=
NM_001427.4:c.686-991C= MANE Select NP_001418.2:n.686-991C=
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