Canonical Allele Identifier: CA2733799878
Gene: DLX4 HGNC NCBI

Linked Data

dbSNP Id: rs2144165649

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974224del , CM000679.2:g.49974224del GRCh38
NC_000017.10:g.48051588del , CM000679.1:g.48051588del GRCh37
NC_000017.9:g.45406587del NCBI36
NG_030592.1:g.10027del

Transcript Alleles

HGVS Amino-acid change
ENST00000706528.1:n.1885del
ENST00000240306.5:c.*281del MANE Select ENSP00000240306.3:n.*281del
ENST00000240306.4:c.*281del ENSP00000240306.3:n.*281del
ENST00000411890.3:c.*281del ENSP00000410622.2:n.*281del
ENST00000611342.1:c.*874del ENSP00000480366.1:n.*874del
NM_001934.3:c.*281del NP_001925.2:n.*281del
NM_138281.2:c.*281del NP_612138.1:n.*281del
XM_011524459.1:c.*281del XP_011522761.1:n.*281del
XM_017024291.1:c.*281del XP_016879780.1:n.*281del
NM_138281.3:c.*281del MANE Select NP_612138.1:n.*281del
NM_001934.4:c.*281del NP_001925.2:n.*281del