Canonical Allele Identifier: CA772784217
Gene: DLX4 HGNC NCBI

Linked Data

dbSNP Id: rs1191257619

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974200dup , CM000679.2:g.49974200dup GRCh38
NC_000017.10:g.48051564dup , CM000679.1:g.48051564dup GRCh37
NC_000017.9:g.45406563dup NCBI36
NG_030592.1:g.10003dup

Transcript Alleles

HGVS Amino-acid change
ENST00000706528.1:n.1861dup
ENST00000240306.5:c.*257dup MANE Select ENSP00000240306.3:n.*257dup
ENST00000240306.4:c.*257dup ENSP00000240306.3:n.*257dup
ENST00000411890.3:c.*257dup ENSP00000410622.2:n.*257dup
ENST00000611342.1:c.*850dup ENSP00000480366.1:n.*850dup
NM_001934.3:c.*257dup NP_001925.2:n.*257dup
NM_138281.2:c.*257dup NP_612138.1:n.*257dup
XM_011524459.1:c.*257dup XP_011522761.1:n.*257dup
XM_017024291.1:c.*257dup XP_016879780.1:n.*257dup
NM_138281.3:c.*257dup MANE Select NP_612138.1:n.*257dup
NM_001934.4:c.*257dup NP_001925.2:n.*257dup