Canonical Allele Identifier: CA2638666332

Gene: DLX4

Linked Data

• gnomAD v4: 17-49974124-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974124A>G , CM000679.2:g.49974124A>G	GRCh38
NC_000017.10:g.48051488A>G , CM000679.1:g.48051488A>G	GRCh37
NC_000017.9:g.45406487A>G	NCBI36
NG_030592.1:g.9927A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1785A>G
ENST00000240306.5:c.*181A>G MANE Select	ENSP00000240306.3:n.*181A>G
ENST00000240306.4:c.*181A>G	ENSP00000240306.3:n.*181A>G
ENST00000411890.3:c.*181A>G	ENSP00000410622.2:n.*181A>G
ENST00000611342.1:c.*774A>G	ENSP00000480366.1:n.*774A>G
NM_001934.3:c.*181A>G	NP_001925.2:n.*181A>G
NM_138281.2:c.*181A>G	NP_612138.1:n.*181A>G
XM_011524459.1:c.*181A>G	XP_011522761.1:n.*181A>G
XM_017024291.1:c.*181A>G	XP_016879780.1:n.*181A>G
NM_138281.3:c.*181A>G MANE Select	NP_612138.1:n.*181A>G
NM_001934.4:c.*181A>G	NP_001925.2:n.*181A>G