Canonical Allele Identifier: CA2263822000
Gene: DLX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991823T= , CM000679.2:g.49991823T= GRCh38
NC_000017.10:g.48069187T= , CM000679.1:g.48069187T= GRCh37
NC_000017.9:g.45424186T= NCBI36
NG_023063.1:g.8402A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000434704.2:c.558A= MANE Select ENSP00000389870.2:p.Lys186=
ENST00000512495.2:c.198A= ENSP00000449976.1:p.Lys66=
NM_005220.2:c.558A= NP_005211.1:p.Lys186=
XM_011524458.1:c.516+1577A= XP_011522760.1:n.516+1577A=
NM_005220.3:c.558A= MANE Select NP_005211.1:p.Lys186=