Canonical Allele Identifier: CA2264360617
Community Standard Title: NC_000017.11:g.51153539C=
Gene: NME1 HGNC NCBI
NME1-NME2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.51153539C= , CM000679.2:g.51153539C= GRCh38
NC_000017.10:g.49230900C= , CM000679.1:g.49230900C= GRCh37
NC_000017.9:g.46585899C= NCBI36
NG_021169.1:g.4981C=

Transcript Alleles

HGVS Amino-acid Change
NM_001018136.2:c.-128C= (NME1-NME2) NP_001018146.1:n.-128C=
NR_037149.1:n.4C= (NME1-NME2)
ENST00000393196.7:c.-128C= (NME1) ENSP00000376892.3:n.-128C=