Canonical Allele Identifier: CA2263813901
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973921T= , CM000679.2:g.49973921T= GRCh38
NC_000017.10:g.48051285T= , CM000679.1:g.48051285T= GRCh37
NC_000017.9:g.45406284T= NCBI36
NG_030592.1:g.9724T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1582T=
ENST00000240306.5:c.701T= MANE Select ENSP00000240306.3:p.Leu234=
ENST00000240306.4:c.701T= ENSP00000240306.3:p.Leu234=
ENST00000411890.3:c.485T= ENSP00000410622.2:p.Leu162=
ENST00000611342.1:c.*571T= ENSP00000480366.1:n.*571T=
NM_001934.3:c.485T= NP_001925.2:p.Leu162=
NM_138281.2:c.701T= NP_612138.1:p.Leu234=
XM_011524459.1:c.485T= XP_011522761.1:p.Leu162=
XM_017024291.1:c.485T= XP_016879780.1:p.Leu162=
NM_138281.3:c.701T= MANE Select NP_612138.1:p.Leu234=
NM_001934.4:c.485T= NP_001925.2:p.Leu162=