Canonical Allele Identifier: CA2263813839
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973786G= , CM000679.2:g.49973786G= GRCh38
NC_000017.10:g.48051150G= , CM000679.1:g.48051150G= GRCh37
NC_000017.9:g.45406149G= NCBI36
NG_030592.1:g.9589G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1447G=
ENST00000240306.5:c.566G= MANE Select ENSP00000240306.3:p.Gly189=
ENST00000240306.4:c.566G= ENSP00000240306.3:p.Gly189=
ENST00000411890.3:c.350G= ENSP00000410622.2:p.Gly117=
ENST00000611342.1:c.*436G= ENSP00000480366.1:n.*436G=
NM_001934.3:c.350G= NP_001925.2:p.Gly117=
NM_138281.2:c.566G= NP_612138.1:p.Gly189=
XM_011524459.1:c.350G= XP_011522761.1:p.Gly117=
XM_017024291.1:c.350G= XP_016879780.1:p.Gly117=
NM_138281.3:c.566G= MANE Select NP_612138.1:p.Gly189=
NM_001934.4:c.350G= NP_001925.2:p.Gly117=