Canonical Allele Identifier: CA2263813865
Gene: DLX4 HGNC NCBI

Linked Data

dbSNP Id: rs1905617648

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973833del , CM000679.2:g.49973833del GRCh38
NC_000017.10:g.48051197del , CM000679.1:g.48051197del GRCh37
NC_000017.9:g.45406196del NCBI36
NG_030592.1:g.9636del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1494del
ENST00000240306.5:c.613del MANE Select ENSP00000240306.3:p.Trp205GlyfsTer?
ENST00000240306.4:c.613del ENSP00000240306.3:p.Trp205GlyfsTer?
ENST00000411890.3:c.397del ENSP00000410622.2:p.Trp133GlyfsTer?
ENST00000611342.1:c.*483del ENSP00000480366.1:n.*483del
NM_001934.3:c.397del NP_001925.2:p.Trp133GlyfsTer?
NM_138281.2:c.613del NP_612138.1:p.Trp205GlyfsTer?
XM_011524459.1:c.397del XP_011522761.1:p.Trp133GlyfsTer?
XM_017024291.1:c.397del XP_016879780.1:p.Trp133GlyfsTer?
NM_138281.3:c.613del MANE Select NP_612138.1:p.Trp205GlyfsTer?
NM_001934.4:c.397del NP_001925.2:p.Trp133GlyfsTer?