Canonical Allele Identifier: CA400168508
Gene: DLX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973835G>T , CM000679.2:g.49973835G>T GRCh38
NC_000017.10:g.48051199G>T , CM000679.1:g.48051199G>T GRCh37
NC_000017.9:g.45406198G>T NCBI36
NG_030592.1:g.9638G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1496G>T
ENST00000240306.5:c.615G>T MANE Select ENSP00000240306.3:p.Trp205Cys
ENST00000240306.4:c.615G>T ENSP00000240306.3:p.Trp205Cys
ENST00000411890.3:c.399G>T ENSP00000410622.2:p.Trp133Cys
ENST00000611342.1:c.*485G>T ENSP00000480366.1:n.*485G>T
NM_001934.3:c.399G>T NP_001925.2:p.Trp133Cys
NM_138281.2:c.615G>T NP_612138.1:p.Trp205Cys
XM_011524459.1:c.399G>T XP_011522761.1:p.Trp133Cys
XM_017024291.1:c.399G>T XP_016879780.1:p.Trp133Cys
NM_138281.3:c.615G>T MANE Select NP_612138.1:p.Trp205Cys
NM_001934.4:c.399G>T NP_001925.2:p.Trp133Cys