Canonical Allele Identifier: CA2576333635
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974033del , CM000679.2:g.49974033del GRCh38
NC_000017.10:g.48051397del , CM000679.1:g.48051397del GRCh37
NC_000017.9:g.45406396del NCBI36
NG_030592.1:g.9836del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1694del
ENST00000240306.5:c.*90del MANE Select ENSP00000240306.3:n.*90del
ENST00000240306.4:c.*90del ENSP00000240306.3:n.*90del
ENST00000411890.3:c.*90del ENSP00000410622.2:n.*90del
ENST00000611342.1:c.*683del ENSP00000480366.1:n.*683del
NM_001934.3:c.*90del NP_001925.2:n.*90del
NM_138281.2:c.*90del NP_612138.1:n.*90del
XM_011524459.1:c.*90del XP_011522761.1:n.*90del
XM_017024291.1:c.*90del XP_016879780.1:n.*90del
NM_138281.3:c.*90del MANE Select NP_612138.1:n.*90del
NM_001934.4:c.*90del NP_001925.2:n.*90del