Canonical Allele Identifier: CA2263813996
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974135C= , CM000679.2:g.49974135C= GRCh38
NC_000017.10:g.48051499C= , CM000679.1:g.48051499C= GRCh37
NC_000017.9:g.45406498C= NCBI36
NG_030592.1:g.9938C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1796C=
ENST00000240306.5:c.*192C= MANE Select ENSP00000240306.3:n.*192C=
ENST00000240306.4:c.*192C= ENSP00000240306.3:n.*192C=
ENST00000411890.3:c.*192C= ENSP00000410622.2:n.*192C=
ENST00000611342.1:c.*785C= ENSP00000480366.1:n.*785C=
NM_001934.3:c.*192C= NP_001925.2:n.*192C=
NM_138281.2:c.*192C= NP_612138.1:n.*192C=
XM_011524459.1:c.*192C= XP_011522761.1:n.*192C=
XM_017024291.1:c.*192C= XP_016879780.1:n.*192C=
NM_138281.3:c.*192C= MANE Select NP_612138.1:n.*192C=
NM_001934.4:c.*192C= NP_001925.2:n.*192C=