Canonical Allele Identifier: CA2638666498
Gene: DLX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974215_49974216del , CM000679.2:g.49974215_49974216del GRCh38
NC_000017.10:g.48051579_48051580del , CM000679.1:g.48051579_48051580del GRCh37
NC_000017.9:g.45406578_45406579del NCBI36
NG_030592.1:g.10018_10019del

Transcript Alleles

HGVS Amino-acid change
ENST00000706528.1:n.1876_1877del
ENST00000240306.5:c.*272_*273del MANE Select ENSP00000240306.3:n.*272_*273del
ENST00000240306.4:c.*272_*273del ENSP00000240306.3:n.*272_*273del
ENST00000411890.3:c.*272_*273del ENSP00000410622.2:n.*272_*273del
ENST00000611342.1:c.*865_*866del ENSP00000480366.1:n.*865_*866del
NM_001934.3:c.*272_*273del NP_001925.2:n.*272_*273del
NM_138281.2:c.*272_*273del NP_612138.1:n.*272_*273del
XM_011524459.1:c.*272_*273del XP_011522761.1:n.*272_*273del
XM_017024291.1:c.*272_*273del XP_016879780.1:n.*272_*273del
NM_138281.3:c.*272_*273del MANE Select NP_612138.1:n.*272_*273del
NM_001934.4:c.*272_*273del NP_001925.2:n.*272_*273del