Canonical Allele Identifier: CA2638666716
Gene: DLX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974317del , CM000679.2:g.49974317del GRCh38
NC_000017.10:g.48051681del , CM000679.1:g.48051681del GRCh37
NC_000017.9:g.45406680del NCBI36
NG_030592.1:g.10120del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1978del
ENST00000240306.5:c.*374del MANE Select ENSP00000240306.3:n.*374del
ENST00000240306.4:c.*374del ENSP00000240306.3:n.*374del
ENST00000411890.3:c.*374del ENSP00000410622.2:n.*374del
ENST00000611342.1:c.*967del ENSP00000480366.1:n.*967del
NM_001934.3:c.*374del NP_001925.2:n.*374del
NM_138281.2:c.*374del NP_612138.1:n.*374del
XM_011524459.1:c.*374del XP_011522761.1:n.*374del
XM_017024291.1:c.*374del XP_016879780.1:n.*374del
NM_138281.3:c.*374del MANE Select NP_612138.1:n.*374del
NM_001934.4:c.*374del NP_001925.2:n.*374del