Canonical Allele Identifier: CA2638666141
Gene: DLX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973836del , CM000679.2:g.49973836del GRCh38
NC_000017.10:g.48051200del , CM000679.1:g.48051200del GRCh37
NC_000017.9:g.45406199del NCBI36
NG_030592.1:g.9639del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1497del
ENST00000240306.5:c.616del MANE Select ENSP00000240306.3:p.Asp206IlefsTer?
ENST00000240306.4:c.616del ENSP00000240306.3:p.Asp206IlefsTer?
ENST00000411890.3:c.400del ENSP00000410622.2:p.Asp134IlefsTer?
ENST00000611342.1:c.*486del ENSP00000480366.1:n.*486del
NM_001934.3:c.400del NP_001925.2:p.Asp134IlefsTer?
NM_138281.2:c.616del NP_612138.1:p.Asp206IlefsTer?
XM_011524459.1:c.400del XP_011522761.1:p.Asp134IlefsTer?
XM_017024291.1:c.400del XP_016879780.1:p.Asp134IlefsTer?
NM_138281.3:c.616del MANE Select NP_612138.1:p.Asp206IlefsTer?
NM_001934.4:c.400del NP_001925.2:p.Asp134IlefsTer?