Canonical Allele Identifier: CA2263813900
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973914G= , CM000679.2:g.49973914G= GRCh38
NC_000017.10:g.48051278G= , CM000679.1:g.48051278G= GRCh37
NC_000017.9:g.45406277G= NCBI36
NG_030592.1:g.9717G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1575G=
ENST00000240306.5:c.694G= MANE Select ENSP00000240306.3:p.Asp232=
ENST00000240306.4:c.694G= ENSP00000240306.3:p.Asp232=
ENST00000411890.3:c.478G= ENSP00000410622.2:p.Asp160=
ENST00000611342.1:c.*564G= ENSP00000480366.1:n.*564G=
NM_001934.3:c.478G= NP_001925.2:p.Asp160=
NM_138281.2:c.694G= NP_612138.1:p.Asp232=
XM_011524459.1:c.478G= XP_011522761.1:p.Asp160=
XM_017024291.1:c.478G= XP_016879780.1:p.Asp160=
NM_138281.3:c.694G= MANE Select NP_612138.1:p.Asp232=
NM_001934.4:c.478G= NP_001925.2:p.Asp160=