Canonical Allele Identifier: CA2263814056
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974273_49974276delinsCCTT , CM000679.2:g.49974273_49974276delinsCCTT GRCh38
NC_000017.10:g.48051637_48051640delinsCCTT , CM000679.1:g.48051637_48051640delinsCCTT GRCh37
NC_000017.9:g.45406636_45406639delinsCCTT NCBI36
NG_030592.1:g.10076_10079delinsCCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1934_1937delinsCCTT
ENST00000240306.5:c.*330_*333delinsCCTT MANE Select ENSP00000240306.3:n.*330_*333delinsCCTT
ENST00000240306.4:c.*330_*333delinsCCTT ENSP00000240306.3:n.*330_*333delinsCCTT
ENST00000411890.3:c.*330_*333delinsCCTT ENSP00000410622.2:n.*330_*333delinsCCTT
ENST00000611342.1:c.*923_*926delinsCCTT ENSP00000480366.1:n.*923_*926delinsCCTT
NM_001934.3:c.*330_*333delinsCCTT NP_001925.2:n.*330_*333delinsCCTT
NM_138281.2:c.*330_*333delinsCCTT NP_612138.1:n.*330_*333delinsCCTT
XM_011524459.1:c.*330_*333delinsCCTT XP_011522761.1:n.*330_*333delinsCCTT
XM_017024291.1:c.*330_*333delinsCCTT XP_016879780.1:n.*330_*333delinsCCTT
NM_138281.3:c.*330_*333delinsCCTT MANE Select NP_612138.1:n.*330_*333delinsCCTT
NM_001934.4:c.*330_*333delinsCCTT NP_001925.2:n.*330_*333delinsCCTT