Canonical Allele Identifier: CA2263814033
Gene: DLX4 HGNC NCBI

Linked Data

dbSNP Id: rs1905636149
gnomAD v4: 17-49974229-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974229G>A , CM000679.2:g.49974229G>A GRCh38
NC_000017.10:g.48051593G>A , CM000679.1:g.48051593G>A GRCh37
NC_000017.9:g.45406592G>A NCBI36
NG_030592.1:g.10032G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706528.1:n.1890G>A
ENST00000240306.5:c.*286G>A MANE Select ENSP00000240306.3:n.*286G>A
ENST00000240306.4:c.*286G>A ENSP00000240306.3:n.*286G>A
ENST00000411890.3:c.*286G>A ENSP00000410622.2:n.*286G>A
ENST00000611342.1:c.*879G>A ENSP00000480366.1:n.*879G>A
NM_001934.3:c.*286G>A NP_001925.2:n.*286G>A
NM_138281.2:c.*286G>A NP_612138.1:n.*286G>A
XM_011524459.1:c.*286G>A XP_011522761.1:n.*286G>A
XM_017024291.1:c.*286G>A XP_016879780.1:n.*286G>A
NM_138281.3:c.*286G>A MANE Select NP_612138.1:n.*286G>A
NM_001934.4:c.*286G>A NP_001925.2:n.*286G>A
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