Canonical Allele Identifier: CA2638666306
Gene: DLX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974112_49974117del , CM000679.2:g.49974112_49974117del GRCh38
NC_000017.10:g.48051476_48051481del , CM000679.1:g.48051476_48051481del GRCh37
NC_000017.9:g.45406475_45406480del NCBI36
NG_030592.1:g.9915_9920del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1773_1778del
ENST00000240306.5:c.*169_*174del MANE Select ENSP00000240306.3:n.*169_*174del
ENST00000240306.4:c.*169_*174del ENSP00000240306.3:n.*169_*174del
ENST00000411890.3:c.*169_*174del ENSP00000410622.2:n.*169_*174del
ENST00000611342.1:c.*762_*767del ENSP00000480366.1:n.*762_*767del
NM_001934.3:c.*169_*174del NP_001925.2:n.*169_*174del
NM_138281.2:c.*169_*174del NP_612138.1:n.*169_*174del
XM_011524459.1:c.*169_*174del XP_011522761.1:n.*169_*174del
XM_017024291.1:c.*169_*174del XP_016879780.1:n.*169_*174del
NM_138281.3:c.*169_*174del MANE Select NP_612138.1:n.*169_*174del
NM_001934.4:c.*169_*174del NP_001925.2:n.*169_*174del