Canonical Allele Identifier: CA2263813853
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973820C= , CM000679.2:g.49973820C= GRCh38
NC_000017.10:g.48051184C= , CM000679.1:g.48051184C= GRCh37
NC_000017.9:g.45406183C= NCBI36
NG_030592.1:g.9623C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1481C=
ENST00000240306.5:c.600C= MANE Select ENSP00000240306.3:p.Pro200=
ENST00000240306.4:c.600C= ENSP00000240306.3:p.Pro200=
ENST00000411890.3:c.384C= ENSP00000410622.2:p.Pro128=
ENST00000611342.1:c.*470C= ENSP00000480366.1:n.*470C=
NM_001934.3:c.384C= NP_001925.2:p.Pro128=
NM_138281.2:c.600C= NP_612138.1:p.Pro200=
XM_011524459.1:c.384C= XP_011522761.1:p.Pro128=
XM_017024291.1:c.384C= XP_016879780.1:p.Pro128=
NM_138281.3:c.600C= MANE Select NP_612138.1:p.Pro200=
NM_001934.4:c.384C= NP_001925.2:p.Pro128=