Canonical Allele Identifier: CA2263813888
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973889A= , CM000679.2:g.49973889A= GRCh38
NC_000017.10:g.48051253A= , CM000679.1:g.48051253A= GRCh37
NC_000017.9:g.45406252A= NCBI36
NG_030592.1:g.9692A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1550A=
ENST00000240306.5:c.669A= MANE Select ENSP00000240306.3:p.Gly223=
ENST00000240306.4:c.669A= ENSP00000240306.3:p.Gly223=
ENST00000411890.3:c.453A= ENSP00000410622.2:p.Gly151=
ENST00000611342.1:c.*539A= ENSP00000480366.1:n.*539A=
NM_001934.3:c.453A= NP_001925.2:p.Gly151=
NM_138281.2:c.669A= NP_612138.1:p.Gly223=
XM_011524459.1:c.453A= XP_011522761.1:p.Gly151=
XM_017024291.1:c.453A= XP_016879780.1:p.Gly151=
NM_138281.3:c.669A= MANE Select NP_612138.1:p.Gly223=
NM_001934.4:c.453A= NP_001925.2:p.Gly151=