Canonical Allele Identifier: CA400174729
Gene: DLX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991831A>T , CM000679.2:g.49991831A>T GRCh38
NC_000017.10:g.48069195A>T , CM000679.1:g.48069195A>T GRCh37
NC_000017.9:g.45424194A>T NCBI36
NG_023063.1:g.8394T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000434704.2:c.550T>A MANE Select ENSP00000389870.2:p.Phe184Ile
ENST00000512495.2:c.190T>A ENSP00000449976.1:p.Phe64Ile
NM_005220.2:c.550T>A NP_005211.1:p.Phe184Ile
XM_011524458.1:c.516+1569T>A XP_011522760.1:n.516+1569T>A
NM_005220.3:c.550T>A MANE Select NP_005211.1:p.Phe184Ile