Canonical Allele Identifier: CA2263813902
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973923G= , CM000679.2:g.49973923G= GRCh38
NC_000017.10:g.48051287G= , CM000679.1:g.48051287G= GRCh37
NC_000017.9:g.45406286G= NCBI36
NG_030592.1:g.9726G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1584G=
ENST00000240306.5:c.703G= MANE Select ENSP00000240306.3:p.Ala235=
ENST00000240306.4:c.703G= ENSP00000240306.3:p.Ala235=
ENST00000411890.3:c.487G= ENSP00000410622.2:p.Ala163=
ENST00000611342.1:c.*573G= ENSP00000480366.1:n.*573G=
NM_001934.3:c.487G= NP_001925.2:p.Ala163=
NM_138281.2:c.703G= NP_612138.1:p.Ala235=
XM_011524459.1:c.487G= XP_011522761.1:p.Ala163=
XM_017024291.1:c.487G= XP_016879780.1:p.Ala163=
NM_138281.3:c.703G= MANE Select NP_612138.1:p.Ala235=
NM_001934.4:c.487G= NP_001925.2:p.Ala163=