Canonical Allele Identifier: CA2638666359
Gene: DLX4 HGNC NCBI

Linked Data

gnomAD v4: 17-49974139-CT-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974141del , CM000679.2:g.49974141del GRCh38
NC_000017.10:g.48051505del , CM000679.1:g.48051505del GRCh37
NC_000017.9:g.45406504del NCBI36
NG_030592.1:g.9944del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1802del
ENST00000240306.5:c.*198del MANE Select ENSP00000240306.3:n.*198del
ENST00000240306.4:c.*198del ENSP00000240306.3:n.*198del
ENST00000411890.3:c.*198del ENSP00000410622.2:n.*198del
ENST00000611342.1:c.*791del ENSP00000480366.1:n.*791del
NM_001934.3:c.*198del NP_001925.2:n.*198del
NM_138281.2:c.*198del NP_612138.1:n.*198del
XM_011524459.1:c.*198del XP_011522761.1:n.*198del
XM_017024291.1:c.*198del XP_016879780.1:n.*198del
NM_138281.3:c.*198del MANE Select NP_612138.1:n.*198del
NM_001934.4:c.*198del NP_001925.2:n.*198del
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