Canonical Allele Identifier: CA2263813875
Gene: DLX4 HGNC NCBI

Linked Data

dbSNP Id: rs1905618750

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973848_49973854del , CM000679.2:g.49973848_49973854del GRCh38
NC_000017.10:g.48051212_48051218del , CM000679.1:g.48051212_48051218del GRCh37
NC_000017.9:g.45406211_45406217del NCBI36
NG_030592.1:g.9651_9657del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1509_1515del
ENST00000240306.5:c.628_634del MANE Select ENSP00000240306.3:p.Ala210ProfsTer28
ENST00000240306.4:c.628_634del ENSP00000240306.3:p.Ala210ProfsTer28
ENST00000411890.3:c.412_418del ENSP00000410622.2:p.Ala138ProfsTer28
ENST00000611342.1:c.*498_*504del ENSP00000480366.1:n.*498_*504del
NM_001934.3:c.412_418del NP_001925.2:p.Ala138ProfsTer28
NM_138281.2:c.628_634del NP_612138.1:p.Ala210ProfsTer28
XM_011524459.1:c.412_418del XP_011522761.1:p.Ala138ProfsTer28
XM_017024291.1:c.412_418del XP_016879780.1:p.Ala138ProfsTer28
NM_138281.3:c.628_634del MANE Select NP_612138.1:p.Ala210ProfsTer28
NM_001934.4:c.412_418del NP_001925.2:p.Ala138ProfsTer28