Canonical Allele Identifier: CA2263821958
Gene: DLX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991721G= , CM000679.2:g.49991721G= GRCh38
NC_000017.10:g.48069085G= , CM000679.1:g.48069085G= GRCh37
NC_000017.9:g.45424084G= NCBI36
NG_023063.1:g.8504C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000434704.2:c.660C= MANE Select ENSP00000389870.2:p.Ser220=
ENST00000512495.2:c.300C= ENSP00000449976.1:p.Ser100=
NM_005220.2:c.660C= NP_005211.1:p.Ser220=
XM_011524458.1:c.516+1679C= XP_011522760.1:n.516+1679C=
NM_005220.3:c.660C= MANE Select NP_005211.1:p.Ser220=