Canonical Allele Identifier: CA2263813852
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973817A= , CM000679.2:g.49973817A= GRCh38
NC_000017.10:g.48051181A= , CM000679.1:g.48051181A= GRCh37
NC_000017.9:g.45406180A= NCBI36
NG_030592.1:g.9620A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1478A=
ENST00000240306.5:c.597A= MANE Select ENSP00000240306.3:p.Pro199=
ENST00000240306.4:c.597A= ENSP00000240306.3:p.Pro199=
ENST00000411890.3:c.381A= ENSP00000410622.2:p.Pro127=
ENST00000611342.1:c.*467A= ENSP00000480366.1:n.*467A=
NM_001934.3:c.381A= NP_001925.2:p.Pro127=
NM_138281.2:c.597A= NP_612138.1:p.Pro199=
XM_011524459.1:c.381A= XP_011522761.1:p.Pro127=
XM_017024291.1:c.381A= XP_016879780.1:p.Pro127=
NM_138281.3:c.597A= MANE Select NP_612138.1:p.Pro199=
NM_001934.4:c.381A= NP_001925.2:p.Pro127=