Canonical Allele Identifier: CA656370902
Gene: DLX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974288_49974289insT , CM000679.2:g.49974288_49974289insT GRCh38
NC_000017.10:g.48051652_48051653insT , CM000679.1:g.48051652_48051653insT GRCh37
NC_000017.9:g.45406651_45406652insT NCBI36
NG_030592.1:g.10091_10092insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1949_1950insT
ENST00000240306.5:c.*345_*346insT MANE Select ENSP00000240306.3:n.*345_*346insT
ENST00000240306.4:c.*345_*346insT ENSP00000240306.3:n.*345_*346insT
ENST00000411890.3:c.*345_*346insT ENSP00000410622.2:n.*345_*346insT
ENST00000611342.1:c.*938_*939insT ENSP00000480366.1:n.*938_*939insT
NM_001934.3:c.*345_*346insT NP_001925.2:n.*345_*346insT
NM_138281.2:c.*345_*346insT NP_612138.1:n.*345_*346insT
XM_011524459.1:c.*345_*346insT XP_011522761.1:n.*345_*346insT
XM_017024291.1:c.*345_*346insT XP_016879780.1:n.*345_*346insT
NM_138281.3:c.*345_*346insT MANE Select NP_612138.1:n.*345_*346insT
NM_001934.4:c.*345_*346insT NP_001925.2:n.*345_*346insT