Canonical Allele Identifier: CA2263821960
Gene: DLX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991723A= , CM000679.2:g.49991723A= GRCh38
NC_000017.10:g.48069087A= , CM000679.1:g.48069087A= GRCh37
NC_000017.9:g.45424086A= NCBI36
NG_023063.1:g.8502T=

Transcript Alleles

HGVS Amino-acid change
ENST00000434704.2:c.658T= MANE Select ENSP00000389870.2:p.Ser220=
ENST00000512495.2:c.298T= ENSP00000449976.1:p.Ser100=
NM_005220.2:c.658T= NP_005211.1:p.Ser220=
XM_011524458.1:c.516+1677T= XP_011522760.1:n.516+1677T=
NM_005220.3:c.658T= MANE Select NP_005211.1:p.Ser220=