Canonical Allele Identifier: CA2264360622
Gene: NME1 HGNC NCBI
NME1-NME2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.51153551G= , CM000679.2:g.51153551G= GRCh38
NC_000017.10:g.49230912G= , CM000679.1:g.49230912G= GRCh37
NC_000017.9:g.46585911G= NCBI36
NG_021169.1:g.4993G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393196.7:c.-116G= (NME1) ENSP00000376892.3:n.-116G=
NM_001018136.2:c.-116G= (NME1-NME2) NP_001018146.1:n.-116G=
NR_037149.1:n.16G= (NME1-NME2)