Canonical Allele Identifier: CA2263813885
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973884T= , CM000679.2:g.49973884T= GRCh38
NC_000017.10:g.48051248T= , CM000679.1:g.48051248T= GRCh37
NC_000017.9:g.45406247T= NCBI36
NG_030592.1:g.9687T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1545T=
ENST00000240306.5:c.664T= MANE Select ENSP00000240306.3:p.Phe222=
ENST00000240306.4:c.664T= ENSP00000240306.3:p.Phe222=
ENST00000411890.3:c.448T= ENSP00000410622.2:p.Phe150=
ENST00000611342.1:c.*534T= ENSP00000480366.1:n.*534T=
NM_001934.3:c.448T= NP_001925.2:p.Phe150=
NM_138281.2:c.664T= NP_612138.1:p.Phe222=
XM_011524459.1:c.448T= XP_011522761.1:p.Phe150=
XM_017024291.1:c.448T= XP_016879780.1:p.Phe150=
NM_138281.3:c.664T= MANE Select NP_612138.1:p.Phe222=
NM_001934.4:c.448T= NP_001925.2:p.Phe150=