Canonical Allele Identifier: CA2638666186
Gene: DLX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974012_49974013insAGCCCAGGACCCAGGCAGT , CM000679.2:g.49974012_49974013insAGCCCAGGACCCAGGCAGT GRCh38
NC_000017.10:g.48051376_48051377insAGCCCAGGACCCAGGCAGT , CM000679.1:g.48051376_48051377insAGCCCAGGACCCAGGCAGT GRCh37
NC_000017.9:g.45406375_45406376insAGCCCAGGACCCAGGCAGT NCBI36
NG_030592.1:g.9815_9816insAGCCCAGGACCCAGGCAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1673_1674insAGCCCAGGACCCAGGCAGT
ENST00000240306.5:c.*69_*70insAGCCCAGGACCCAGGCAGT MANE Select ENSP00000240306.3:n.*69_*70insAGCCCAGGACCCAGGCAGT
ENST00000240306.4:c.*69_*70insAGCCCAGGACCCAGGCAGT ENSP00000240306.3:n.*69_*70insAGCCCAGGACCCAGGCAGT
ENST00000411890.3:c.*69_*70insAGCCCAGGACCCAGGCAGT ENSP00000410622.2:n.*69_*70insAGCCCAGGACCCAGGCAGT
ENST00000611342.1:c.*662_*663insAGCCCAGGACCCAGGCAGT ENSP00000480366.1:n.*662_*663insAGCCCAGGACCCAGGCAGT
NM_001934.3:c.*69_*70insAGCCCAGGACCCAGGCAGT NP_001925.2:n.*69_*70insAGCCCAGGACCCAGGCAGT
NM_138281.2:c.*69_*70insAGCCCAGGACCCAGGCAGT NP_612138.1:n.*69_*70insAGCCCAGGACCCAGGCAGT
XM_011524459.1:c.*69_*70insAGCCCAGGACCCAGGCAGT XP_011522761.1:n.*69_*70insAGCCCAGGACCCAGGCAGT
XM_017024291.1:c.*69_*70insAGCCCAGGACCCAGGCAGT XP_016879780.1:n.*69_*70insAGCCCAGGACCCAGGCAGT
NM_138281.3:c.*69_*70insAGCCCAGGACCCAGGCAGT MANE Select NP_612138.1:n.*69_*70insAGCCCAGGACCCAGGCAGT
NM_001934.4:c.*69_*70insAGCCCAGGACCCAGGCAGT NP_001925.2:n.*69_*70insAGCCCAGGACCCAGGCAGT