Canonical Allele Identifier: CA2263813842
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973793C= , CM000679.2:g.49973793C= GRCh38
NC_000017.10:g.48051157C= , CM000679.1:g.48051157C= GRCh37
NC_000017.9:g.45406156C= NCBI36
NG_030592.1:g.9596C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1454C=
ENST00000240306.5:c.573C= MANE Select ENSP00000240306.3:p.Thr191=
ENST00000240306.4:c.573C= ENSP00000240306.3:p.Thr191=
ENST00000411890.3:c.357C= ENSP00000410622.2:p.Thr119=
ENST00000611342.1:c.*443C= ENSP00000480366.1:n.*443C=
NM_001934.3:c.357C= NP_001925.2:p.Thr119=
NM_138281.2:c.573C= NP_612138.1:p.Thr191=
XM_011524459.1:c.357C= XP_011522761.1:p.Thr119=
XM_017024291.1:c.357C= XP_016879780.1:p.Thr119=
NM_138281.3:c.573C= MANE Select NP_612138.1:p.Thr191=
NM_001934.4:c.357C= NP_001925.2:p.Thr119=