Canonical Allele Identifier: CA2638666510
Gene: DLX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974218_49974221dup , CM000679.2:g.49974218_49974221dup GRCh38
NC_000017.10:g.48051582_48051585dup , CM000679.1:g.48051582_48051585dup GRCh37
NC_000017.9:g.45406581_45406584dup NCBI36
NG_030592.1:g.10021_10024dup

Transcript Alleles

HGVS Amino-acid change
ENST00000706528.1:n.1879_1882dup
ENST00000240306.5:c.*275_*278dup MANE Select ENSP00000240306.3:n.*275_*278dup
ENST00000240306.4:c.*275_*278dup ENSP00000240306.3:n.*275_*278dup
ENST00000411890.3:c.*275_*278dup ENSP00000410622.2:n.*275_*278dup
ENST00000611342.1:c.*868_*871dup ENSP00000480366.1:n.*868_*871dup
NM_001934.3:c.*275_*278dup NP_001925.2:n.*275_*278dup
NM_138281.2:c.*275_*278dup NP_612138.1:n.*275_*278dup
XM_011524459.1:c.*275_*278dup XP_011522761.1:n.*275_*278dup
XM_017024291.1:c.*275_*278dup XP_016879780.1:n.*275_*278dup
NM_138281.3:c.*275_*278dup MANE Select NP_612138.1:n.*275_*278dup
NM_001934.4:c.*275_*278dup NP_001925.2:n.*275_*278dup