Canonical Allele Identifier: CA2263814065
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974300T= , CM000679.2:g.49974300T= GRCh38
NC_000017.10:g.48051664T= , CM000679.1:g.48051664T= GRCh37
NC_000017.9:g.45406663T= NCBI36
NG_030592.1:g.10103T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1961T=
ENST00000240306.5:c.*357T= MANE Select ENSP00000240306.3:n.*357T=
ENST00000240306.4:c.*357T= ENSP00000240306.3:n.*357T=
ENST00000411890.3:c.*357T= ENSP00000410622.2:n.*357T=
ENST00000611342.1:c.*950T= ENSP00000480366.1:n.*950T=
NM_001934.3:c.*357T= NP_001925.2:n.*357T=
NM_138281.2:c.*357T= NP_612138.1:n.*357T=
XM_011524459.1:c.*357T= XP_011522761.1:n.*357T=
XM_017024291.1:c.*357T= XP_016879780.1:n.*357T=
NM_138281.3:c.*357T= MANE Select NP_612138.1:n.*357T=
NM_001934.4:c.*357T= NP_001925.2:n.*357T=