Canonical Allele Identifier: CA2263821961
Gene: DLX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991727G= , CM000679.2:g.49991727G= GRCh38
NC_000017.10:g.48069091G= , CM000679.1:g.48069091G= GRCh37
NC_000017.9:g.45424090G= NCBI36
NG_023063.1:g.8498C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000434704.2:c.654C= MANE Select ENSP00000389870.2:p.Thr218=
ENST00000512495.2:c.294C= ENSP00000449976.1:p.Thr98=
NM_005220.2:c.654C= NP_005211.1:p.Thr218=
XM_011524458.1:c.516+1673C= XP_011522760.1:n.516+1673C=
NM_005220.3:c.654C= MANE Select NP_005211.1:p.Thr218=