Canonical Allele Identifier: CA2638666324
Gene: DLX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974118del , CM000679.2:g.49974118del GRCh38
NC_000017.10:g.48051482del , CM000679.1:g.48051482del GRCh37
NC_000017.9:g.45406481del NCBI36
NG_030592.1:g.9921del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1779del
ENST00000240306.5:c.*175del MANE Select ENSP00000240306.3:n.*175del
ENST00000240306.4:c.*175del ENSP00000240306.3:n.*175del
ENST00000411890.3:c.*175del ENSP00000410622.2:n.*175del
ENST00000611342.1:c.*768del ENSP00000480366.1:n.*768del
NM_001934.3:c.*175del NP_001925.2:n.*175del
NM_138281.2:c.*175del NP_612138.1:n.*175del
XM_011524459.1:c.*175del XP_011522761.1:n.*175del
XM_017024291.1:c.*175del XP_016879780.1:n.*175del
NM_138281.3:c.*175del MANE Select NP_612138.1:n.*175del
NM_001934.4:c.*175del NP_001925.2:n.*175del