Canonical Allele Identifier: CA2263814102
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974402A= , CM000679.2:g.49974402A= GRCh38
NC_000017.10:g.48051766A= , CM000679.1:g.48051766A= GRCh37
NC_000017.9:g.45406765A= NCBI36
NG_030592.1:g.10205A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.2063A=
ENST00000240306.5:c.*459A= MANE Select ENSP00000240306.3:n.*459A=
ENST00000240306.4:c.*459A= ENSP00000240306.3:n.*459A=
ENST00000411890.3:c.*459A= ENSP00000410622.2:n.*459A=
ENST00000611342.1:c.*1052A= ENSP00000480366.1:n.*1052A=
NM_001934.3:c.*459A= NP_001925.2:n.*459A=
NM_138281.2:c.*459A= NP_612138.1:n.*459A=
XM_011524459.1:c.*459A= XP_011522761.1:n.*459A=
XM_017024291.1:c.*459A= XP_016879780.1:n.*459A=
NM_138281.3:c.*459A= MANE Select NP_612138.1:n.*459A=
NM_001934.4:c.*459A= NP_001925.2:n.*459A=