Canonical Allele Identifier: CA2263813915
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973942G= , CM000679.2:g.49973942G= GRCh38
NC_000017.10:g.48051306G= , CM000679.1:g.48051306G= GRCh37
NC_000017.9:g.45406305G= NCBI36
NG_030592.1:g.9745G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1603G=
ENST00000240306.5:c.722G= MANE Select ENSP00000240306.3:p.Ter241=
ENST00000240306.4:c.722G= ENSP00000240306.3:p.Ter241=
ENST00000411890.3:c.506G= ENSP00000410622.2:p.Ter169=
ENST00000611342.1:c.*592G= ENSP00000480366.1:n.*592G=
NM_001934.3:c.506G= NP_001925.2:p.Ter169=
NM_138281.2:c.722G= NP_612138.1:p.Ter241=
XM_011524459.1:c.506G= XP_011522761.1:p.Ter169=
XM_017024291.1:c.506G= XP_016879780.1:p.Ter169=
NM_138281.3:c.722G= MANE Select NP_612138.1:p.Ter241=
NM_001934.4:c.506G= NP_001925.2:p.Ter169=