Canonical Allele Identifier: CA2263813988
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974111C= , CM000679.2:g.49974111C= GRCh38
NC_000017.10:g.48051475C= , CM000679.1:g.48051475C= GRCh37
NC_000017.9:g.45406474C= NCBI36
NG_030592.1:g.9914C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1772C=
ENST00000240306.5:c.*168C= MANE Select ENSP00000240306.3:n.*168C=
ENST00000240306.4:c.*168C= ENSP00000240306.3:n.*168C=
ENST00000411890.3:c.*168C= ENSP00000410622.2:n.*168C=
ENST00000611342.1:c.*761C= ENSP00000480366.1:n.*761C=
NM_001934.3:c.*168C= NP_001925.2:n.*168C=
NM_138281.2:c.*168C= NP_612138.1:n.*168C=
XM_011524459.1:c.*168C= XP_011522761.1:n.*168C=
XM_017024291.1:c.*168C= XP_016879780.1:n.*168C=
NM_138281.3:c.*168C= MANE Select NP_612138.1:n.*168C=
NM_001934.4:c.*168C= NP_001925.2:n.*168C=